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rs864622585

From SNPedia

ClinVar
Risk rs864622585(T;T)
Alt rs864622585(T;T)
Reference rs864622585(GGTAA;GGTAA)
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.48027430_48027434delGGTAAinsT
CLNSRC
CLNACC RCV000204888.1, RCV000218163.1,