ClinVar Miner

List of variants reported as pathogenic for colorectal cancer by Division of Medical Genetics, University of Washington

Included ClinVar conditions (75):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_000179.3(MSH6):c.3261dup (p.Phe1088fs) rs267608078
NM_000179.3(MSH6):c.706_707del (p.Gln236fs) rs1553412129
NM_000249.4(MLH1):c.1400del (p.Ser467fs) rs1064795515
NM_000251.3(MSH2):c.793-1G>A rs863225397
NM_000535.7(PMS2):c.2117del (p.Lys706fs) rs587782704

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