ClinVar Miner

List of variants reported as likely benign for Lynch syndrome by DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center

Included ClinVar conditions (17):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_000179.2(MSH6):c.1449G>T (p.Val483=) rs35590297
NM_000251.2(MSH2):c.1737A>G (p.Lys579=) rs61756467
NM_000251.2(MSH2):c.2400A>G (p.Leu800=) rs201298777
NM_000251.2(MSH2):c.471C>A (p.Gly157=) rs61756463
NM_000251.2(MSH2):c.984C>T (p.Ala328=) rs4987189
NM_000535.5(PMS2):c.*17G>C rs556089649
NM_000535.6(PMS2):c.1711C>A (p.Leu571Ile) rs63750055

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