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rs863225388

From SNPedia

ClinVar
Risk rs863225388(AGTT;AGTT)
Alt rs863225388(AGTT;AGTT)
Reference Rs863225388(TATACAGGCTCTGGAAAA;TATACAGGCTCTGGAAAA)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47657055_47657072del18insAGTT
CLNSRC
CLNACC RCV000202139.1, RCV000491837.1,