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rs786203893

From SNPedia

ClinVar
Risk rs786203893(;)
Alt rs786203893(;)
Reference rs786203893(TTCTAGTGGCAGGGCTA;TTCTAGTGGCAGGGCTA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37067346_37067362del17
CLNSRC
CLNACC RCV000167395.1,