"Ambry Genetics"[submitter] AND "LOC126861068"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2329859	NM_001377530.1(DMBT1):c.6986C>T (p.Ala2329Val)	DMBT1, LOC126861068 (A2200V +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2510815	NM_001377530.1(DMBT1):c.7033G>A (p.Val2345Ile)	DMBT1, LOC126861068 (V2345I +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2371327	NM_001377530.1(DMBT1):c.7066G>A (p.Asp2356Asn)	DMBT1, LOC126861068 (D2217N +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2383970	NM_001377530.1(DMBT1):c.7078A>G (p.Ile2360Val)	DMBT1, LOC126861068 (I2231V +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2464530	NM_001377530.1(DMBT1):c.7123G>A (p.Glu2375Lys)	DMBT1, LOC126861068 (E1618K +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2538350	NM_001377530.1(DMBT1):c.7324T>C (p.Ser2442Pro)	DMBT1, LOC126861068 (S2312P +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar