ClinVar for Gene (Select 120892) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 3348

<< First< Prev

Page of 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3253534	NM_198578.4(LRRK2):c.6280+1G>A	LRRK2	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 3244313	NC_000012.11:g.(?_40681133)_(40681361_?)dup	LRRK2	Duplication	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 3229806	NM_198578.4(LRRK2):c.908C>T (p.Pro303Leu)	LRRK2 (P303L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229805	NM_198578.4(LRRK2):c.843T>G (p.Asn281Lys)	LRRK2 (N281K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229804	NM_198578.4(LRRK2):c.842A>T (p.Asn281Ile)	LRRK2 (N281I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229803	NM_198578.4(LRRK2):c.805G>A (p.Val269Met)	LRRK2 (V269M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229802	NM_198578.4(LRRK2):c.759G>C (p.Val253=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229801	NM_198578.4(LRRK2):c.756T>C (p.Ile252=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229800	NM_198578.4(LRRK2):c.7541G>A (p.Arg2514Lys)	LRRK2 (R2514K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229799	NM_198578.4(LRRK2):c.7537G>A (p.Val2513Met)	LRRK2 (V2513M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229798	NM_198578.4(LRRK2):c.7531A>G (p.Ile2511Val)	LRRK2 (I2511V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229797	NM_198578.4(LRRK2):c.7530C>T (p.His2510=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229796	NM_198578.4(LRRK2):c.7525A>G (p.Lys2509Glu)	LRRK2 (K2509E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229795	NM_198578.4(LRRK2):c.7508A>T (p.Glu2503Val)	LRRK2 (E2503V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229794	NM_198578.4(LRRK2):c.7465A>C (p.Ile2489Leu)	LRRK2 (I2489L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229793	NM_198578.4(LRRK2):c.7463A>T (p.Glu2488Val)	LRRK2 (E2488V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229792	NM_198578.4(LRRK2):c.7436A>T (p.Asn2479Ile)	LRRK2 (N2479I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229791	NM_198578.4(LRRK2):c.7419G>C (p.Leu2473Phe)	LRRK2 (L2473F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229790	NM_198578.4(LRRK2):c.740T>C (p.Val247Ala)	LRRK2 (V247A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229789	NM_198578.4(LRRK2):c.7400A>G (p.Lys2467Arg)	LRRK2 (K2467R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229788	NM_198578.4(LRRK2):c.7395C>G (p.Ser2465Arg)	LRRK2 (S2465R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229787	NM_198578.4(LRRK2):c.7373T>C (p.Met2458Thr)	LRRK2 (M2458T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229786	NM_198578.4(LRRK2):c.734G>A (p.Gly245Asp)	LRRK2 (G245D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229785	NM_198578.4(LRRK2):c.7349A>C (p.Asn2450Thr)	LRRK2 (N2450T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229784	NM_198578.4(LRRK2):c.7306C>T (p.Leu2436Phe)	LRRK2 (L2436F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229783	NM_198578.4(LRRK2):c.7268C>T (p.Thr2423Ile)	LRRK2 (T2423I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229782	NM_198578.4(LRRK2):c.7249C>A (p.Leu2417Ile)	LRRK2 (L2417I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229781	NM_198578.4(LRRK2):c.7240G>T (p.Val2414Leu)	LRRK2 (V2414L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229780	NM_198578.4(LRRK2):c.7238G>A (p.Arg2413Lys)	LRRK2 (R2413K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229779	NM_198578.4(LRRK2):c.7221A>G (p.Lys2407=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229778	NM_198578.4(LRRK2):c.7187T>C (p.Val2396Ala)	LRRK2 (V2396A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229777	NM_198578.4(LRRK2):c.7170G>A (p.Val2390=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229776	NM_198578.4(LRRK2):c.7165T>A (p.Cys2389Ser)	LRRK2 (C2389S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229775	NM_198578.4(LRRK2):c.715G>T (p.Val239Leu)	LRRK2 (V239L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229774	NM_198578.4(LRRK2):c.7139C>T (p.Thr2380Ile)	LRRK2 (T2380I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229773	NM_198578.4(LRRK2):c.7138A>G (p.Thr2380Ala)	LRRK2 (T2380A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229772	NM_198578.4(LRRK2):c.7109G>T (p.Ser2370Ile)	LRRK2 (S2370I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229771	NM_198578.4(LRRK2):c.7087C>A (p.Leu2363Ile)	LRRK2 (L2363I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229770	NM_198578.4(LRRK2):c.7052A>G (p.Asp2351Gly)	LRRK2 (D2351G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229769	NM_198578.4(LRRK2):c.7027C>A (p.Leu2343Met)	LRRK2 (L2343M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229768	NM_198578.4(LRRK2):c.7019C>T (p.Thr2340Ile)	LRRK2 (T2340I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229767	NM_198578.4(LRRK2):c.7019C>A (p.Thr2340Lys)	LRRK2 (T2340K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229766	NM_198578.4(LRRK2):c.6997C>G (p.Gln2333Glu)	LRRK2 (Q2333E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229765	NM_198578.4(LRRK2):c.6975C>T (p.Ser2325=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229764	NM_198578.4(LRRK2):c.6954A>T (p.Gly2318=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229763	NM_198578.4(LRRK2):c.6951A>G (p.Gly2317=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229762	NM_198578.4(LRRK2):c.6913G>C (p.Glu2305Gln)	LRRK2 (E2305Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229761	NM_198578.4(LRRK2):c.6851G>A (p.Gly2284Glu)	LRRK2 (G2284E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229760	NM_198578.4(LRRK2):c.6844C>G (p.Leu2282Val)	LRRK2 (L2282V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229759	NM_198578.4(LRRK2):c.6816A>G (p.Leu2272=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229758	NM_198578.4(LRRK2):c.680A>G (p.His227Arg)	LRRK2 (H227R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229756	NM_198578.4(LRRK2):c.6778A>G (p.Lys2260Glu)	LRRK2 (K2260E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229755	NM_198578.4(LRRK2):c.6778A>C (p.Lys2260Gln)	LRRK2 (K2260Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229754	NM_198578.4(LRRK2):c.6745T>C (p.Tyr2249His)	LRRK2 (Y2249H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229753	NM_198578.4(LRRK2):c.6737C>G (p.Thr2246Ser)	LRRK2 (T2246S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229752	NM_198578.4(LRRK2):c.6710C>T (p.Thr2237Ile)	LRRK2 (T2237I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229751	NM_198578.4(LRRK2):c.6708T>C (p.His2236=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229750	NM_198578.4(LRRK2):c.6701A>G (p.Lys2234Arg)	LRRK2 (K2234R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229749	NM_198578.4(LRRK2):c.669T>A (p.Leu223=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229748	NM_198578.4(LRRK2):c.6694G>C (p.Gly2232Arg)	LRRK2 (G2232R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229747	NM_198578.4(LRRK2):c.6675G>C (p.Leu2225=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229746	NM_198578.4(LRRK2):c.6662C>G (p.Ser2221Cys)	LRRK2 (S2221C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229745	NM_198578.4(LRRK2):c.6646G>A (p.Val2216Met)	LRRK2 (V2216M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229744	NM_198578.4(LRRK2):c.6643A>T (p.Ile2215Phe)	LRRK2 (I2215F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229743	NM_198578.4(LRRK2):c.6598T>C (p.Leu2200=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229742	NM_198578.4(LRRK2):c.6593G>A (p.Arg2198Lys)	LRRK2 (R2198K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229741	NM_198578.4(LRRK2):c.6581T>C (p.Val2194Ala)	LRRK2 (V2194A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229740	NM_198578.4(LRRK2):c.6577G>A (p.Glu2193Lys)	LRRK2 (E2193K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229739	NM_198578.4(LRRK2):c.6572C>T (p.Ser2191Phe)	LRRK2 (S2191F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229738	NM_198578.4(LRRK2):c.6561A>C (p.Glu2187Asp)	LRRK2 (E2187D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229737	NM_198578.4(LRRK2):c.6553A>G (p.Asn2185Asp)	LRRK2 (N2185D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229736	NM_198578.4(LRRK2):c.6538T>A (p.Ser2180Thr)	LRRK2 (S2180T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229735	NM_198578.4(LRRK2):c.6508G>C (p.Gly2170Arg)	LRRK2 (G2170R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229734	NM_198578.4(LRRK2):c.6498C>G (p.Ser2166Arg)	LRRK2 (S2166R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229733	NM_198578.4(LRRK2):c.6495A>G (p.Ala2165=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229732	NM_198578.4(LRRK2):c.6489G>A (p.Arg2163=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229731	NM_198578.4(LRRK2):c.6481A>C (p.Asn2161His)	LRRK2 (N2161H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229730	NM_198578.4(LRRK2):c.6441T>A (p.Pro2147=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229729	NM_198578.4(LRRK2):c.6385T>C (p.Phe2129Leu)	LRRK2 (F2129L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229728	NM_198578.4(LRRK2):c.6360A>G (p.Gln2120=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229727	NM_198578.4(LRRK2):c.6349G>C (p.Glu2117Gln)	LRRK2 (E2117Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229726	NM_198578.4(LRRK2):c.625T>C (p.Leu209=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229725	NM_198578.4(LRRK2):c.6249T>A (p.Phe2083Leu)	LRRK2 (F2083L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229724	NM_198578.4(LRRK2):c.612T>C (p.Asp204=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229723	NM_198578.4(LRRK2):c.6126A>G (p.Glu2042=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229722	NM_198578.4(LRRK2):c.605A>T (p.Asn202Ile)	LRRK2 (N202I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229721	NM_198578.4(LRRK2):c.6029C>T (p.Ala2010Val)	LRRK2 (A2010V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229720	NM_198578.4(LRRK2):c.6024T>C (p.Asn2008=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229719	NM_198578.4(LRRK2):c.6017A>G (p.Tyr2006Cys)	LRRK2 (Y2006C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229718	NM_198578.4(LRRK2):c.5970T>G (p.Ile1990Met)	LRRK2 (I1990M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229717	NM_198578.4(LRRK2):c.5939A>T (p.Asp1980Val)	LRRK2 (D1980V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229716	NM_198578.4(LRRK2):c.5921T>C (p.Ile1974Thr)	LRRK2 (I1974T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229715	NM_198578.4(LRRK2):c.5894G>A (p.Ser1965Asn)	LRRK2 (S1965N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229714	NM_198578.4(LRRK2):c.5871C>A (p.Arg1957=)	LRRK2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3229713	NM_198578.4(LRRK2):c.5852C>A (p.Ser1951Tyr)	LRRK2 (S1951Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229712	NM_198578.4(LRRK2):c.5830A>T (p.Met1944Leu)	LRRK2 (M1944L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229711	NM_198578.4(LRRK2):c.5782C>T (p.His1928Tyr)	LRRK2 (H1928Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229710	NM_198578.4(LRRK2):c.5744G>A (p.Arg1915Lys)	LRRK2 (R1915K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229709	NM_198578.4(LRRK2):c.5734A>G (p.Thr1912Ala)	LRRK2 (T1912A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3229708	NM_198578.4(LRRK2):c.567G>C (p.Glu189Asp)	LRRK2 (E189D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

<< First< Prev

Page of 34