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rs869312771

From SNPedia

ClinVar
Risk rs869312771(-;-)
Alt rs869312771(-;-)
Reference rs869312771(CAGGGAGGAGAGCTCTGCC;CAGGGAGGAGAGCTCTGCC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45797400_45797418del19
CLNSRC
CLNACC RCV000210110.1,