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rs587779287

From SNPedia

ClinVar
Risk rs587779287(;)
Alt rs587779287(;)
Reference rs587779287(TCGTACATTATTT;TCGTACATTATTT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033421_48033433delGTACATTATTTTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074921.2,