ClinVar Miner

List of variants reported as likely pathogenic for digestive system cancer by CSER _CC_NCGL, University of Washington

Included ClinVar conditions (140):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_000179.3(MSH6):c.892C>T (p.Arg298Ter) rs146816935 0.00001
NM_000535.7(PMS2):c.1144+1G>A rs373885654 0.00001
NM_000251.3(MSH2):c.1571G>C (p.Arg524Pro) rs63751207

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