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rs876658296

From SNPedia

ClinVar
Risk rs876658296(-;-)
Alt rs876658296(-;-)
Reference Rs876658296(GGCCCAGGCCCTT;GGCCCAGGCCCTT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48010542_48010554delCCAGGCCCTTGGC
CLNSRC
CLNACC RCV000215541.1,