ClinVar Miner

List of variants in gene MSH6 reported as benign for Lynch syndrome

Included ClinVar conditions (18):
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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP
MSH6:c.3647-51_3647-35del17 rs267607687
NM_000179.2(MSH6):c.*4247G>A
NM_000179.2(MSH6):c.-159C>T rs41540312
NM_000179.2(MSH6):c.-210C>T rs181096360
NM_000179.2(MSH6):c.-448G>A rs3136229
NM_000179.2(MSH6):c.-557T>G rs3136228
NM_000179.2(MSH6):c.1164C>T (p.His388=) rs55708305
NM_000179.2(MSH6):c.116G>A (p.Gly39Glu) rs1042821
NM_000179.2(MSH6):c.1186C>G (p.Leu396Val) rs2020908
NM_000179.2(MSH6):c.1345C>T (p.Leu449=) rs3136333
NM_000179.2(MSH6):c.1809G>A (p.Lys603=) rs876660790
NM_000179.2(MSH6):c.186C>A (p.Arg62=) rs1042820
NM_000179.2(MSH6):c.2253T>C (p.Asn751=) rs2020913
NM_000179.2(MSH6):c.2272C>T (p.Leu758=) rs56371757
NM_000179.2(MSH6):c.260+2214C>T rs3136245
NM_000179.2(MSH6):c.260+22C>G rs55927047
NM_000179.2(MSH6):c.260+2467A>G rs3136247
NM_000179.2(MSH6):c.261-1170G>T rs3136272
NM_000179.2(MSH6):c.261-36A>G rs1800931
NM_000179.2(MSH6):c.2633T>C (p.Val878Ala) rs2020912
NM_000179.2(MSH6):c.276A>G (p.Pro92=) rs1800932
NM_000179.2(MSH6):c.3172+171C>T rs3136337
NM_000179.2(MSH6):c.3173-101G>C rs2072447
NM_000179.2(MSH6):c.3246G>T (p.Pro1082=) rs3136351
NM_000179.2(MSH6):c.3306T>A (p.Thr1102=) rs2020910
NM_000179.2(MSH6):c.3438+14A>T rs2020911
NM_000179.2(MSH6):c.3439-16C>T rs192614006
NM_000179.2(MSH6):c.3556+146G>A rs7562048
NM_000179.2(MSH6):c.3556+160T>C rs56320267
NM_000179.2(MSH6):c.3557-3A>T rs41295274
NM_000179.2(MSH6):c.3646+35_3646+38del rs1805181
NM_000179.2(MSH6):c.3646+35_3646+38dup rs1805181
NM_000179.2(MSH6):c.3646+91T>C rs3136359
NM_000179.2(MSH6):c.3647-35_3647-34insTTTGTTCTAATTCCTTT rs397515292
NM_000179.2(MSH6):c.3802-40C>G rs3136367
NM_000179.2(MSH6):c.3852G>T (p.Thr1284=) rs2229018
NM_000179.2(MSH6):c.4002-10del rs59056100
NM_000179.2(MSH6):c.4002-11_4002-10dup rs59056100
NM_000179.2(MSH6):c.4002-12_4002-10dup rs59056100
NM_000179.2(MSH6):c.4002-13_4002-10dup rs59056100
NM_000179.2(MSH6):c.431G>T (p.Ser144Ile) rs3211299
NM_000179.2(MSH6):c.457+1223T>C rs2348244
NM_000179.2(MSH6):c.457+13A>G rs1800933
NM_000179.2(MSH6):c.457+394T>C rs3136284
NM_000179.2(MSH6):c.457+52T>A rs3136282
NM_000179.2(MSH6):c.458-52G>T rs1800934
NM_000179.2(MSH6):c.540T>C (p.Asp180=) rs1800935
NM_000179.2(MSH6):c.627+1200T>C rs3136326
NM_000179.2(MSH6):c.628-56C>T rs1800936
NM_000179.2(MSH6):c.628-874C>T rs3136329
NM_000179.2(MSH6):c.642C>T (p.Tyr214=) rs1800937
NM_001281492.1(MSH6):c.3167-4dup rs267608102
NM_001281492.1(MSH6):c.3412-43dup rs34154602

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