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

rs864621967

From SNPedia

ClinVar
Risk rs864621967(;)
Alt rs864621967(;)
Reference rs864621967(GGCACTA;GGCACTA)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MUTYH
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.45796848_45796854delTAGTGCC
CLNSRC
CLNACC RCV000160747.2, RCV000215481.1,