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

rs796053242

From SNPedia

ClinVar
Risk rs796053242(;)
Alt rs796053242(;)
Reference rs796053242(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC25A22
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.792310_792311delAG
CLNSRC
CLNACC RCV000189333.1,