ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as uncertain significance by GeneDx

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Total variants: 50
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HGVS dbSNP
NM_001365536.1(SCN9A):c.1022A>G (p.Tyr341Cys) rs374280444
NM_001365536.1(SCN9A):c.1099T>C (p.Tyr367His) rs200457046
NM_001365536.1(SCN9A):c.1109C>T (p.Thr370Met) rs200391162
NM_001365536.1(SCN9A):c.1115G>A (p.Arg372His) rs201071819
NM_001365536.1(SCN9A):c.1280T>C (p.Leu427Ser) rs192406412
NM_001365536.1(SCN9A):c.1304A>C (p.Glu435Ala) rs201396897
NM_001365536.1(SCN9A):c.1555G>A (p.Glu519Lys) rs187453572
NM_001365536.1(SCN9A):c.1619G>A (p.Arg540His) rs199748300
NM_001365536.1(SCN9A):c.1650C>G (p.Ser550Arg) rs200192044
NM_001365536.1(SCN9A):c.1660C>A (p.Leu554Ile) rs201994523
NM_001365536.1(SCN9A):c.1675G>A (p.Gly559Ser) rs201569378
NM_001365536.1(SCN9A):c.1901G>A (p.Arg634His) rs774510851
NM_001365536.1(SCN9A):c.1999A>G (p.Lys667Glu) rs775090142
NM_001365536.1(SCN9A):c.2004G>T (p.Arg668Ser) rs200970256
NM_001365536.1(SCN9A):c.2005C>T (p.Arg669Cys) rs200174262
NM_001365536.1(SCN9A):c.2085A>G (p.Ile695Met) rs199588089
NM_001365536.1(SCN9A):c.2220T>G (p.Ile740Met) rs375688386
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val) rs182650126
NM_001365536.1(SCN9A):c.2299C>A (p.Pro767Thr) rs199715588
NM_001365536.1(SCN9A):c.2351C>G (p.Thr784Ser) rs200624920
NM_001365536.1(SCN9A):c.2461G>A (p.Val821Met) rs41268671
NM_001365536.1(SCN9A):c.2518-10T>G rs879254177
NM_001365536.1(SCN9A):c.2815G>A (p.Ala939Thr) rs1064793264
NM_001365536.1(SCN9A):c.2975T>C (p.Val992Ala) rs1057524814
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys) rs199692186
NM_001365536.1(SCN9A):c.3020G>A (p.Arg1007His) rs188145203
NM_001365536.1(SCN9A):c.3028A>G (p.Ile1010Val) rs375510818
NM_001365536.1(SCN9A):c.3051G>C (p.Lys1017Asn) rs147623238
NM_001365536.1(SCN9A):c.3289G>A (p.Asp1097Asn) rs768654039
NM_001365536.1(SCN9A):c.3322A>G (p.Ser1108Gly) rs758165714
NM_001365536.1(SCN9A):c.3329C>T (p.Ser1110Leu) rs145258166
NM_001365536.1(SCN9A):c.3403C>T (p.Pro1135Ser) rs184563685
NM_001365536.1(SCN9A):c.3598C>T (p.Leu1200Phe) rs201233540
NM_001365536.1(SCN9A):c.3944T>C (p.Ile1315Thr) rs202235611
NM_001365536.1(SCN9A):c.4009A>C (p.Ile1337Leu) rs543167736
NM_001365536.1(SCN9A):c.4289G>A (p.Ser1430Asn) rs201479177
NM_001365536.1(SCN9A):c.4476G>T (p.Lys1492Asn) rs879253974
NM_001365536.1(SCN9A):c.4621C>A (p.Gln1541Lys) rs1064796825
NM_001365536.1(SCN9A):c.4892G>T (p.Arg1631Leu) rs201079869
NM_001365536.1(SCN9A):c.4904T>C (p.Phe1635Ser) rs879254053
NM_001365536.1(SCN9A):c.4965G>T (p.Met1655Ile) rs200166620
NM_001365536.1(SCN9A):c.5086A>T (p.Thr1696Ser) rs879254140
NM_001365536.1(SCN9A):c.5207G>C (p.Gly1736Ala) rs776586182
NM_001365536.1(SCN9A):c.5251G>C (p.Val1751Leu) rs879253908
NM_001365536.1(SCN9A):c.5420C>G (p.Ala1807Gly) rs879254324
NM_001365536.1(SCN9A):c.5561G>A (p.Gly1854Glu) rs876661011
NM_001365536.1(SCN9A):c.5563G>A (p.Glu1855Lys) rs876661248
NM_001365536.1(SCN9A):c.5615C>T (p.Pro1872Leu) rs879254298
NM_001365536.1(SCN9A):c.5711G>A (p.Arg1904His) rs79805025
NM_001365536.1(SCN9A):c.5949C>G (p.Ser1983Arg) rs201640210

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