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

rs797046112

From SNPedia

ClinVar
Risk rs797046112(;)
Alt rs797046112(;)
Reference rs797046112(TCT;TCT)
Significance Probable-Pathogenic
Disease Wolfram syndrome
Variation info
Gene WFS1
CLNDBN Wolfram syndrome
Reversed 0
HGVS NC_000004.11:g.6302762_6302764delTTC
CLNSRC
CLNACC RCV000193337.1,