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rs587782172

From SNPedia

ClinVar
Risk rs587782172(;)
Alt rs587782172(;)
Reference rs587782172(GAGGTGGGACACGGCAA;GAGGTGGGACACGGCAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48023201_48023217del17
CLNSRC
CLNACC RCV000130771.1,