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rs863224829

From SNPedia

ClinVar
Risk rs863224829(;)
Alt rs863224829(;)
Reference rs863224829(AGTA;AGTA)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48026732_48026735delAGTA
CLNSRC
CLNACC RCV000196707.1, RCV000213843.1,