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rs267607702

From SNPedia

ClinVar
Risk
Alt
Reference Rs267607702(GTTATTCGGCGGCTGGA;GTTATTCGGCGGCTGGA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035057_37035073del17
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075476.2,