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

rs121913126

From SNPedia

OMIM137192
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913126(T;T)
Alt rs121913126(T;T)
Reference rs121913126(C;C)
Significance Other
Disease Epilepsy
Variation info
Gene GABRB3
CLNDBN Epilepsy, childhood absence 5
Reversed 1
HGVS NC_000015.9:g.27018828G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017576.2,