ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance for breast disorder

Included ClinVar conditions (69):
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Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_000179.3(MSH6):c.3961A>G (p.Arg1321Gly) rs41295278 0.00019
NM_000179.3(MSH6):c.650A>G (p.Asp217Gly) rs554012110 0.00013
NM_000179.3(MSH6):c.3674C>T (p.Thr1225Met) rs63750370 0.00011
NM_000179.3(MSH6):c.628-7C>A rs373129248 0.00011
NM_000179.3(MSH6):c.2417C>G (p.Ser806Cys) rs372990379 0.00010
NM_000179.3(MSH6):c.335A>G (p.Asn112Ser) rs587779934 0.00010
NM_000179.3(MSH6):c.1063G>A (p.Gly355Ser) rs587778531 0.00009
NM_000179.3(MSH6):c.3425C>T (p.Thr1142Met) rs267608089 0.00005
NM_000179.3(MSH6):c.1364A>C (p.Asn455Thr) rs200938360 0.00004
NM_000179.3(MSH6):c.1937A>G (p.Lys646Arg) rs201096652 0.00004
NM_000179.3(MSH6):c.2408A>G (p.Asp803Gly) rs63751450 0.00004
NM_000179.3(MSH6):c.-6G>C rs730881822 0.00003
NM_000179.3(MSH6):c.3026A>T (p.Lys1009Ile) rs587781593 0.00003
NM_000179.3(MSH6):c.1159G>C (p.Asp387His) rs746532720 0.00002
NM_000179.3(MSH6):c.1493A>G (p.Lys498Arg) rs147136417 0.00002
NM_000179.3(MSH6):c.1773A>G (p.Pro591=) rs752239740 0.00002
NM_000179.3(MSH6):c.2511C>G (p.His837Gln) rs587779925 0.00002
NM_000179.3(MSH6):c.2857G>A (p.Glu953Lys) rs753034685 0.00002
NM_000179.3(MSH6):c.3205G>C (p.Gly1069Arg) rs764113705 0.00002
NM_000179.3(MSH6):c.3759AGA[3] (p.Glu1254dup) rs587779937 0.00002
NM_000179.3(MSH6):c.852T>C (p.Asp284=) rs1057520320 0.00002
NM_000179.3(MSH6):c.-11C>A rs1225209597 0.00001
NM_000179.3(MSH6):c.1277G>A (p.Cys426Tyr) rs1207702287 0.00001
NM_000179.3(MSH6):c.1894A>G (p.Lys632Glu) rs755847154 0.00001
NM_000179.3(MSH6):c.2885T>C (p.Ile962Thr) rs778287080 0.00001
NM_000179.3(MSH6):c.3893A>G (p.Tyr1298Cys) rs786202520 0.00001
NM_000179.3(MSH6):c.533G>A (p.Arg178His) rs786204186 0.00001
NM_000179.3(MSH6):c.667A>G (p.Asn223Asp) rs374041375 0.00001
NM_000179.3(MSH6):c.979A>G (p.Thr327Ala) rs730881814 0.00001
NM_000179.3(MSH6):c.-4C>T rs1114167784
NM_000179.3(MSH6):c.1037C>G (p.Ser346Cys) rs567785169
NM_000179.3(MSH6):c.1752T>C (p.Thr584=) rs1114167777
NM_000179.3(MSH6):c.2132C>T (p.Pro711Leu) rs2104390270
NM_000179.3(MSH6):c.2503C>G (p.Gln835Glu) rs63751321
NM_000179.3(MSH6):c.2505G>C (p.Gln835His) rs863224328
NM_000179.3(MSH6):c.2561_2562delinsTT (p.Lys854Ile) rs587780673
NM_000179.3(MSH6):c.3259C>G (p.Pro1087Ala) rs63750998
NM_000179.3(MSH6):c.3259C>T (p.Pro1087Ser) rs63750998
NM_000179.3(MSH6):c.3299C>T (p.Thr1100Met) rs63750442
NM_000179.3(MSH6):c.339C>T (p.His113=) rs886056141
NM_000179.3(MSH6):c.347A>G (p.Asp116Gly) rs1553410255
NM_000179.3(MSH6):c.3646+5G>A rs1669974239
NM_000179.3(MSH6):c.3758T>A (p.Val1253Glu) rs202066386
NM_000179.3(MSH6):c.3969T>G (p.Phe1323Leu) rs1057520473
NM_000179.3(MSH6):c.432C>T (p.Ser144=) rs1046304919
NM_000179.3(MSH6):c.442T>C (p.Leu148=) rs2104111846
NM_000179.3(MSH6):c.467C>T (p.Ser156Leu) rs63749873

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