Have questions? Visit https://www.reddit.com/r/SNPedia

rs121912626

From SNPedia

OMIM607170
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121912626(G;G)
Alt rs121912626(G;G)
Reference rs121912626(C;C)
Significance Other
Disease Atrioventricular septal defect 2
Variation info
Gene CRELD1
CLNDBN Atrioventricular septal defect 2
Reversed 0
HGVS NC_000003.11:g.9982557C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003599.2,