ClinVar Miner

List of variants reported as uncertain significance for Lynch syndrome by CSER _CC_NCGL, University of Washington

Included ClinVar conditions (18):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_000179.2(MSH6):c.3299C>T (p.Thr1100Met) rs63750442
NM_000179.2(MSH6):c.383G>T (p.Arg128Leu) rs63750143
NM_000249.3(MLH1):c.1637A>G (p.Lys546Arg) rs587779954
NM_000251.2(MSH2):c.1803G>C (p.Gln601His) rs1553368556
NM_000535.7(PMS2):c.1096G>C (p.Asp366His) rs141769057
NM_000535.7(PMS2):c.2466T>C (p.Leu822=) rs10000
NM_000535.7(PMS2):c.944G>A (p.Arg315Gln) rs116314131
NM_001040108.1(MLH3):c.3440A>T (p.Asn1147Ile) rs142124529

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