ClinVar Miner

List of variants reported as uncertain significance for Lynch syndrome by OMIM

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.2633T>C (p.Val878Ala) rs2020912
NM_000249.3(MLH1):c.-93G>A rs1800734
NM_000249.4(MLH1):c.1733A>G (p.Glu578Gly) rs63751612
NM_001040108.1(MLH3):c.1870G>C (p.Glu624Gln) rs28756986
NM_001040108.1(MLH3):c.4351G>A (p.Glu1451Lys) rs28939071
NM_001354630.1(MLH1):c.1732-878_1732-877delinsGC rs35502531
NM_014381.3(MLH3):c.1496A>G (p.Asn499Ser) rs28937871
NM_014381.3(MLH3):c.70C>G (p.Gln24Glu) rs28937870

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