ClinVar Miner

List of variants reported as uncertain significance for Lynch syndrome by Integrated Genetics/Laboratory Corporation of America

Included ClinVar conditions (18):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP
MHS6:c.3647-65_3647-61del rs3136363
NM_000179.2(MSH6):c.38A>C (p.Lys13Thr) rs41294988
NM_000179.2(MSH6):c.553A>G (p.Lys185Glu) rs193922344
NM_000249.3(MLH1):c.1896+17T>C rs193922368
NM_000249.3(MLH1):c.1937A>G (p.Tyr646Cys) rs35045067
NM_000249.3(MLH1):c.80G>C (p.Arg27Pro) rs138705565
NM_000249.3(MLH1):c.94A>G (p.Ile32Val) rs2020872
NM_000251.2(MSH2):c.421A>G (p.Met141Val) rs193922374

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