ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance by International Society for Gastrointestinal Hereditary Tumours (InSiGHT)

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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NM_000179.2(MSH6):c.3338T>G (p.Ile1113Ser) rs41295272
NM_000179.2(MSH6):c.4064_4065insGTCA (p.Leu1356fs) rs267608141

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