ClinVar Miner

List of variants in gene combination LOC102724058, SCN1A reported as likely benign by GeneDx

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Total variants: 65
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HGVS dbSNP
NM_001165963.1(SCN1A):c.4338+18dupT rs1064795145
NM_006920.6(SCN1A):c.3068T>C (p.Ile1023Thr) rs121918818
NM_006920.6(SCN1A):c.3072A>G (p.Gln1024=) rs144013543
NM_006920.6(SCN1A):c.3078C>A (p.Ser1026=) rs1204620691
NM_006920.6(SCN1A):c.3213T>C (p.Thr1071=) rs961517010
NM_006920.6(SCN1A):c.3216A>C (p.Thr1072=) rs1042252202
NM_006920.6(SCN1A):c.3354G>A (p.Thr1118=) rs375953445
NM_006920.6(SCN1A):c.3397-7C>A rs975085305
NM_006920.6(SCN1A):c.3417C>T (p.Ser1139=) rs727504137
NM_006920.6(SCN1A):c.3444C>T (p.Ile1148=) rs761878186
NM_006920.6(SCN1A):c.3447C>A (p.Gly1149=) rs369594817
NM_006920.6(SCN1A):c.3447C>T (p.Gly1149=) rs369594817
NM_006920.6(SCN1A):c.3488C>G (p.Thr1163Ser) rs121918799
NM_006920.6(SCN1A):c.3492T>G (p.Leu1164=) rs1057524122
NM_006920.6(SCN1A):c.3540T>C (p.Cys1180=) rs750943685
NM_006920.6(SCN1A):c.3543T>C (p.Cys1181=) rs150638891
NM_006920.6(SCN1A):c.3552T>C (p.Asn1184=) rs138181528
NM_006920.6(SCN1A):c.3558A>G (p.Glu1186=) rs371596040
NM_006920.6(SCN1A):c.3597G>A (p.Thr1199=) rs377326177
NM_006920.6(SCN1A):c.3605G>A (p.Arg1202Gln) rs566081370
NM_006920.6(SCN1A):c.3672+17A>G rs1553532428
NM_006920.6(SCN1A):c.3673-146C>G
NM_006920.6(SCN1A):c.3673-20G>A rs187973818
NM_006920.6(SCN1A):c.3684T>C (p.Asp1228=) rs376579606
NM_006920.6(SCN1A):c.3708G>A (p.Thr1236=) rs200745708
NM_006920.6(SCN1A):c.3717G>T (p.Thr1239=) rs771494149
NM_006920.6(SCN1A):c.3855G>A (p.Leu1285=) rs998325208
NM_006920.6(SCN1A):c.3891A>T (p.Glu1297Asp) rs121917910
NM_006920.6(SCN1A):c.3970-15C>T rs1057521559
NM_006920.6(SCN1A):c.3970-8T>C rs1553525411
NM_006920.6(SCN1A):c.4062C>T (p.Gly1354=)
NM_006920.6(SCN1A):c.4134C>T (p.Asp1378=) rs376118833
NM_006920.6(SCN1A):c.4251+19C>A rs1383995139
NM_006920.6(SCN1A):c.4305+12T>C rs761062999
NM_006920.6(SCN1A):c.4306-5G>A rs1057522587
NM_006920.6(SCN1A):c.4443+6T>C rs1057523807
NM_006920.6(SCN1A):c.4444-11C>A rs775315152
NM_006920.6(SCN1A):c.4488C>T (p.Tyr1496=) rs750997506
NM_006920.6(SCN1A):c.4518A>G (p.Lys1506=) rs374087499
NM_006920.6(SCN1A):c.4548+124C>G
NM_006920.6(SCN1A):c.4548+12C>T rs886055042
NM_006920.6(SCN1A):c.4549-12A>G rs752455718
NM_006920.6(SCN1A):c.4549-27G>A
NM_006920.6(SCN1A):c.4549-4A>C rs1057521695
NM_006920.6(SCN1A):c.4549-4A>G rs1057521695
NM_006920.6(SCN1A):c.4599C>T (p.Asp1533=) rs1057521371
NM_006920.6(SCN1A):c.4758T>C (p.His1586=) rs141051370
NM_006920.6(SCN1A):c.4837C>T (p.Leu1613=) rs1553520513
NM_006920.6(SCN1A):c.4854C>T (p.Phe1618=) rs587780445
NM_006920.6(SCN1A):c.4872C>T (p.Phe1624=) rs774858072
NM_006920.6(SCN1A):c.4890T>C (p.Ala1630=) rs369650500
NM_006920.6(SCN1A):c.4947C>T (p.Leu1649=) rs1057521307
NM_006920.6(SCN1A):c.4993C>T (p.Leu1665=) rs1553520391
NM_006920.6(SCN1A):c.5094C>A (p.Thr1698=) rs777044331
NM_006920.6(SCN1A):c.5184C>T (p.Pro1728=) rs149315236
NM_006920.6(SCN1A):c.5346T>A (p.Thr1782=) rs1553520152
NM_006920.6(SCN1A):c.5499A>G (p.Pro1833=) rs886043063
NM_006920.6(SCN1A):c.5599_5601delinsAAT (p.Glu1867Asn)
NM_006920.6(SCN1A):c.5623C>A (p.Arg1875=)
NM_006920.6(SCN1A):c.5706A>G (p.Lys1902=) rs554861427
NM_006920.6(SCN1A):c.5730T>C (p.Ile1910=) rs767698089
NM_006920.6(SCN1A):c.5749C>G (p.Arg1917Gly) rs121917956
NM_006920.6(SCN1A):c.5790G>A (p.Thr1930=) rs754371368
NM_006920.6(SCN1A):c.5832A>G (p.Ile1944Met) rs796052952
NM_006920.6(SCN1A):c.5944A>G (p.Ile1982Val) rs751750112

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