ClinVar Miner

List of variants in gene MSH6 reported as likely benign by Mayo Clinic Genetic Testing Laboratories,Mayo Clinic

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Gene type:
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Total variants: 17
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HGVS dbSNP
NM_000179.2(MSH6):c.1449G>T (p.Val483=) rs35590297
NM_000179.2(MSH6):c.2187C>A (p.Ala729=) rs375610656
NM_000179.2(MSH6):c.2239C>T (p.Leu747=) rs63751305
NM_000179.2(MSH6):c.2745C>G (p.Ala915=) rs876658904
NM_000179.2(MSH6):c.2877C>T (p.Arg959=) rs781734958
NM_000179.2(MSH6):c.2904C>G (p.Val968=) rs150683226
NM_000179.2(MSH6):c.3160A>T (p.Ile1054Phe) rs267608075
NM_000179.2(MSH6):c.3173-97T>C rs138463559
NM_000179.2(MSH6):c.3384T>C (p.Tyr1128=) rs544518097
NM_000179.2(MSH6):c.3396T>A (p.Val1132=) rs1026907245
NM_000179.2(MSH6):c.3439-16C>T rs192614006
NM_000179.2(MSH6):c.3557-4del rs267608102
NM_000179.2(MSH6):c.3801+17T>C rs3136365
NM_000179.2(MSH6):c.4001+2TAAC[2] rs267608132
NM_000179.2(MSH6):c.4001+49_4001+50insCTAACTGACCTTAAGTTTCAA rs863225419
NM_000179.2(MSH6):c.4002-25T>C rs199500983
NM_000179.2(MSH6):c.457+13A>G rs1800933

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