ClinVar Miner

List of variants in gene SYNE1 reported as benign by PreventionGenetics

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Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP
NM_033071.3(SYNE1):c.24012A>G (p.Ala8004=) rs910415
NM_033071.3(SYNE1):c.9516A>G (p.Glu3172=) rs6913579
NM_182961.4(SYNE1):c.10191C>A (p.Gly3397=) rs4407724
NM_182961.4(SYNE1):c.1047+4T>A rs9397106
NM_182961.4(SYNE1):c.10866T>C (p.Ser3622=) rs9397102
NM_182961.4(SYNE1):c.11254-31T>G rs6932325
NM_182961.4(SYNE1):c.11580+15C>T rs6908392
NM_182961.4(SYNE1):c.11621A>C (p.Lys3874Thr) rs13210127
NM_182961.4(SYNE1):c.11734-5T>G rs9478320
NM_182961.4(SYNE1):c.1185+46A>G rs58766460
NM_182961.4(SYNE1):c.12000G>A (p.Ala4000=) rs148493518
NM_182961.4(SYNE1):c.12180G>T (p.Glu4060Asp) rs4645434
NM_182961.4(SYNE1):c.12352-39A>G rs9479298
NM_182961.4(SYNE1):c.12362A>G (p.Lys4121Arg) rs9479297
NM_182961.4(SYNE1):c.12795-12A>G rs9478314
NM_182961.4(SYNE1):c.130-25C>T rs2141152
NM_182961.4(SYNE1):c.13221C>T (p.Asp4407=) rs10499268
NM_182961.4(SYNE1):c.1351-24A>T rs4331993
NM_182961.4(SYNE1):c.1351-27T>C rs4343926
NM_182961.4(SYNE1):c.13786T>A (p.Ser4596Thr) rs6911096
NM_182961.4(SYNE1):c.14061G>C (p.Leu4687=) rs3734365
NM_182961.4(SYNE1):c.1463+24G>T rs4523096
NM_182961.4(SYNE1):c.14917C>T (p.Leu4973=) rs35085679
NM_182961.4(SYNE1):c.15043T>A (p.Leu5015Met) rs2306916
NM_182961.4(SYNE1):c.15597C>G (p.Ala5199=) rs9383987
NM_182961.4(SYNE1):c.16572+32G>C rs17082448
NM_182961.4(SYNE1):c.16711-25C>T rs1538
NM_182961.4(SYNE1):c.17202+24G>A rs12662994
NM_182961.4(SYNE1):c.17339G>A (p.Arg5780Gln) rs76160752
NM_182961.4(SYNE1):c.17346+38C>T rs9371581
NM_182961.4(SYNE1):c.17346+7G>A rs9383985
NM_182961.4(SYNE1):c.17745C>T (p.His5915=) rs12664753
NM_182961.4(SYNE1):c.18208-24A>G rs9478310
NM_182961.4(SYNE1):c.19104+17A>G rs17082389
NM_182961.4(SYNE1):c.19471-18C>T rs6557210
NM_182961.4(SYNE1):c.20530-14G>A rs2296254
NM_182961.4(SYNE1):c.20571A>T (p.Ser6857=) rs34905593
NM_182961.4(SYNE1):c.21656+13T>C rs9383976
NM_182961.4(SYNE1):c.21904T>G (p.Phe7302Val) rs2147377
NM_182961.4(SYNE1):c.22191+42G>C rs9371243
NM_182961.4(SYNE1):c.22473G>A (p.Leu7491=) rs34891041
NM_182961.4(SYNE1):c.22671C>T (p.Ile7557=) rs3798756
NM_182961.4(SYNE1):c.22809C>T (p.Leu7603=) rs34630198
NM_182961.4(SYNE1):c.23145+33C>T rs2253512
NM_182961.4(SYNE1):c.23627+29G>A rs41292868
NM_182961.4(SYNE1):c.24450+28A>T rs2348080
NM_182961.4(SYNE1):c.24825G>A (p.Pro8275=) rs2252748
NM_182961.4(SYNE1):c.24968G>C (p.Gly8323Ala) rs2252755
NM_182961.4(SYNE1):c.24977-1682T>C rs2813487
NM_182961.4(SYNE1):c.24977-1774A>G rs2747662
NM_182961.4(SYNE1):c.25038T>C (p.Arg8346=) rs2256135
NM_182961.4(SYNE1):c.25120-16G>T rs139671151
NM_182961.4(SYNE1):c.25458+24C>T rs3818110
NM_182961.4(SYNE1):c.25458+33_25458+36del rs147380321
NM_182961.4(SYNE1):c.26060C>T (p.Thr8687Ile) rs35591210
NM_182961.4(SYNE1):c.2653T>G (p.Leu885Val) rs17082709
NM_182961.4(SYNE1):c.2728-25C>T rs214968
NM_182961.4(SYNE1):c.3104T>C (p.Val1035Ala) rs214976
NM_182961.4(SYNE1):c.3306C>T (p.His1102=) rs17082701
NM_182961.4(SYNE1):c.3505-39A>C rs502268
NM_182961.4(SYNE1):c.5190T>A (p.Asp1730Glu) rs111250109
NM_182961.4(SYNE1):c.7029+45T>C rs177330
NM_182961.4(SYNE1):c.7030-21T>A rs79428643
NM_182961.4(SYNE1):c.7713-49G>A rs214944
NM_182961.4(SYNE1):c.8163C>T (p.Ser2721=) rs58905396
NM_182961.4(SYNE1):c.8177+20A>T rs214943
NM_182961.4(SYNE1):c.8177+9C>T rs56877632
NM_182961.4(SYNE1):c.8384C>T (p.Ala2795Val) rs214950
NM_182961.4(SYNE1):c.9147-13G>A rs214955
NM_182961.4(SYNE1):c.9651+47C>T rs1873176
NM_182961.4(SYNE1):c.9808-50G>A rs7775637
NM_182961.4(SYNE1):c.9972+19A>G rs77322999

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