ClinVar Miner

List of variants reported as likely pathogenic for Lynch syndrome by Pathway Genomics

Included ClinVar conditions (18):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_000251.2(MSH2):c.2304del (p.Glu768fs) rs587783053
NM_000251.2(MSH2):c.2363_2364del (p.Thr788fs) rs63750937
NM_000535.7(PMS2):c.1A>G (p.Met1Val) rs587779333
NM_000535.7(PMS2):c.2184_2185TC[1] (p.Leu729fs) rs587779335

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