ClinVar Miner

List of variants reported as benign for Lynch syndrome by IntelligeneCG

Included ClinVar conditions (17):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_000179.2(MSH6):c.116G>A (p.Gly39Glu) rs1042821
NM_000249.3(MLH1):c.655A>G (p.Ile219Val) rs1799977
NM_000535.6(PMS2):c.1408C>T (p.Pro470Ser) rs1805321
NM_000535.6(PMS2):c.1621A>G (p.Lys541Glu) rs2228006
NM_002354.2(EPCAM):c.344T>C (p.Met115Thr) rs1126497

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