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

rs876658296

From SNPedia

ClinVar
Risk rs876658296(;)
Alt rs876658296(;)
Reference rs876658296(GGCCCAGGCCCTT;GGCCCAGGCCCTT)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48010542_48010554delCCAGGCCCTTGGC
CLNSRC
CLNACC RCV000215541.1,