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

rs796053332

From SNPedia

ClinVar
Risk rs796053332(;)
Alt rs796053332(;)
Reference rs796053332(CTC;CTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTAN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131348132_131348134delCTC
CLNSRC
CLNACC RCV000189541.1,