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_002977.3(SCN9A):c.1022A>G (p.Tyr341Cys) rs374280444
NM_002977.3(SCN9A):c.1099T>C (p.Tyr367His) rs200457046
NM_002977.3(SCN9A):c.1109C>T (p.Thr370Met) rs200391162
NM_002977.3(SCN9A):c.1115G>A (p.Arg372His) rs201071819
NM_002977.3(SCN9A):c.1280T>C (p.Leu427Ser) rs192406412
NM_002977.3(SCN9A):c.1304A>C (p.Glu435Ala) rs201396897
NM_002977.3(SCN9A):c.1555G>A (p.Glu519Lys) rs187453572
NM_002977.3(SCN9A):c.1619G>A (p.Arg540His) rs199748300
NM_002977.3(SCN9A):c.1650C>G (p.Ser550Arg) rs200192044
NM_002977.3(SCN9A):c.1660C>A (p.Leu554Ile) rs201994523
NM_002977.3(SCN9A):c.1675G>A (p.Gly559Ser) rs201569378
NM_002977.3(SCN9A):c.1901G>A (p.Arg634His) rs774510851
NM_002977.3(SCN9A):c.1966A>G (p.Lys656Glu) rs775090142
NM_002977.3(SCN9A):c.1971G>T (p.Arg657Ser) rs200970256
NM_002977.3(SCN9A):c.1972C>T (p.Arg658Cys) rs200174262
NM_002977.3(SCN9A):c.2052A>G (p.Ile684Met) rs199588089
NM_002977.3(SCN9A):c.2187T>G (p.Ile729Met) rs375688386
NM_002977.3(SCN9A):c.2215A>G (p.Ile739Val) rs182650126
NM_002977.3(SCN9A):c.2266C>A (p.Pro756Thr) rs199715588
NM_002977.3(SCN9A):c.2318C>G (p.Thr773Ser) rs200624920
NM_002977.3(SCN9A):c.2428G>A (p.Val810Met) rs41268671
NM_002977.3(SCN9A):c.2485-10T>G rs879254177
NM_002977.3(SCN9A):c.2782G>A (p.Ala928Thr) rs1064793264
NM_002977.3(SCN9A):c.2942T>C (p.Val981Ala) rs1057524814
NM_002977.3(SCN9A):c.2969A>G (p.Tyr990Cys) rs199692186
NM_002977.3(SCN9A):c.2987G>A (p.Arg996His) rs188145203
NM_002977.3(SCN9A):c.2995A>G (p.Ile999Val) rs375510818
NM_002977.3(SCN9A):c.3018G>C (p.Lys1006Asn) rs147623238
NM_002977.3(SCN9A):c.3256G>A (p.Asp1086Asn) rs768654039
NM_002977.3(SCN9A):c.3289A>G (p.Ser1097Gly) rs758165714
NM_002977.3(SCN9A):c.3296C>T (p.Ser1099Leu) rs145258166
NM_002977.3(SCN9A):c.3370C>T (p.Pro1124Ser) rs184563685
NM_002977.3(SCN9A):c.3565C>T (p.Leu1189Phe) rs201233540
NM_002977.3(SCN9A):c.3911T>C (p.Ile1304Thr) rs202235611
NM_002977.3(SCN9A):c.3976A>C (p.Ile1326Leu) rs543167736
NM_002977.3(SCN9A):c.4256G>A (p.Ser1419Asn) rs201479177
NM_002977.3(SCN9A):c.4443G>T (p.Lys1481Asn) rs879253974
NM_002977.3(SCN9A):c.4588C>A (p.Gln1530Lys) rs1064796825
NM_002977.3(SCN9A):c.4859G>T (p.Arg1620Leu) rs201079869
NM_002977.3(SCN9A):c.4871T>C (p.Phe1624Ser) rs879254053
NM_002977.3(SCN9A):c.4932G>T (p.Met1644Ile) rs200166620
NM_002977.3(SCN9A):c.5053A>T (p.Thr1685Ser) rs879254140
NM_002977.3(SCN9A):c.5174G>C (p.Gly1725Ala) rs776586182
NM_002977.3(SCN9A):c.5218G>C (p.Val1740Leu) rs879253908
NM_002977.3(SCN9A):c.5387C>G (p.Ala1796Gly) rs879254324
NM_002977.3(SCN9A):c.5528G>A (p.Gly1843Glu) rs876661011
NM_002977.3(SCN9A):c.5530G>A (p.Glu1844Lys) rs876661248
NM_002977.3(SCN9A):c.5582C>T (p.Pro1861Leu) rs879254298
NM_002977.3(SCN9A):c.5678G>A (p.Arg1893His) rs79805025
NM_002977.3(SCN9A):c.5916C>G (p.Ser1972Arg) rs201640210

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