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

rs876659208

From SNPedia

ClinVar
Risk rs876659208(;)
Alt rs876659208(;)
Reference rs876659208(AG;AG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000016.9:g.68849573_68849574delAG
CLNSRC
CLNACC RCV000213871.1,