Related gene-specific medical variations for Gene (Select 4005) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290976	NM_005574.4(LMO2):c.103G>A (p.Gly35Ser)	LMO2, LOC130005521 (G35S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3119354	NM_005574.4(LMO2):c.91G>A (p.Asp31Asn)	LMO2, LOC130005521 (D31N)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3119351	NM_005574.4(LMO2):c.31C>G (p.Arg11Gly)	LMO2, LOC130005522 (R11G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3119349	NM_005574.4(LMO2):c.128G>A (p.Gly43Glu)	LMO2, LOC130005521 (G43E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2594878	NM_005574.4(LMO2):c.25C>T (p.Leu9Phe)	LOC130005522, LMO2 (L9F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2569372	NM_005574.4(LMO2):c.52G>C (p.Ala18Pro)	LMO2, LOC130005522 (A18P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2490080	NM_005574.4(LMO2):c.14C>T (p.Ala5Val)	LMO2, LOC130005522 (A5V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

ClinVar