ClinVar Miner

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

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Total variants: 110
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HGVS dbSNP gnomAD frequency
NM_001365536.1(SCN9A):c.3051G>C (p.Lys1017Asn) rs147623238 0.00149
NM_001365536.1(SCN9A):c.3403C>T (p.Pro1135Ser) rs184563685 0.00081
NM_001365536.1(SCN9A):c.1109C>T (p.Thr370Met) rs200391162 0.00068
NM_001365536.1(SCN9A):c.3329C>T (p.Ser1110Leu) rs145258166 0.00066
NM_001365536.1(SCN9A):c.1555G>A (p.Glu519Lys) rs187453572 0.00059
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys) rs199692186 0.00056
NM_001365536.1(SCN9A):c.3402G>T (p.Leu1134Phe) rs200160858 0.00052
NM_001365536.1(SCN9A):c.3167A>G (p.Lys1056Arg) rs200560768 0.00048
NM_001365536.1(SCN9A):c.1277T>A (p.Met426Lys) rs200415928 0.00046
NM_001365536.1(SCN9A):c.2005C>T (p.Arg669Cys) rs200174262 0.00038
NM_001365536.1(SCN9A):c.3343A>G (p.Ser1115Gly) rs201984007 0.00025
NM_001365536.1(SCN9A):c.2192T>A (p.Ile731Lys) rs200945460 0.00019
NM_001365536.1(SCN9A):c.2220T>G (p.Ile740Met) rs375688386 0.00016
NM_001365536.1(SCN9A):c.1846G>A (p.Gly616Arg) rs201338643 0.00014
NM_001365536.1(SCN9A):c.1675G>A (p.Gly559Ser) rs201569378 0.00013
NM_001365536.1(SCN9A):c.1099T>C (p.Tyr367His) rs200457046 0.00011
NM_001365536.1(SCN9A):c.3482G>A (p.Trp1161Ter) rs759003928 0.00011
NM_001365536.1(SCN9A):c.2085A>G (p.Ile695Met) rs199588089 0.00009
NM_001365536.1(SCN9A):c.3349G>T (p.Val1117Leu) rs200817435 0.00009
NM_001365536.1(SCN9A):c.3028A>G (p.Ile1010Val) rs375510818 0.00008
NM_001365536.1(SCN9A):c.3944T>C (p.Ile1315Thr) rs202235611 0.00007
NM_001365536.1(SCN9A):c.1280T>C (p.Leu427Ser) rs192406412 0.00006
NM_001365536.1(SCN9A):c.2006G>A (p.Arg669His) rs200374987 0.00006
NM_001365536.1(SCN9A):c.3301A>G (p.Met1101Val) rs201699621 0.00006
NM_001365536.1(SCN9A):c.4892G>T (p.Arg1631Leu) rs201079869 0.00006
NM_001365536.1(SCN9A):c.1115G>A (p.Arg372His) rs201071819 0.00005
NM_001365536.1(SCN9A):c.1135A>G (p.Met379Val) rs544004654 0.00005
NM_001365536.1(SCN9A):c.2299C>A (p.Pro767Thr) rs199715588 0.00005
NM_001365536.1(SCN9A):c.902-2A>C rs773824421 0.00005
NM_001365536.1(SCN9A):c.1331C>T (p.Ala444Val) rs143430080 0.00004
NM_001365536.1(SCN9A):c.2242C>G (p.Leu748Val) rs764893083 0.00004
NM_001365536.1(SCN9A):c.2351C>G (p.Thr784Ser) rs200624920 0.00004
NM_001365536.1(SCN9A):c.1604C>T (p.Ser535Leu) rs201354321 0.00003
NM_001365536.1(SCN9A):c.1660C>A (p.Leu554Ile) rs201994523 0.00003
NM_001365536.1(SCN9A):c.3038C>A (p.Ala1013Glu) rs202153871 0.00003
NM_001365536.1(SCN9A):c.4289G>A (p.Ser1430Asn) rs201479177 0.00003
NM_001365536.1(SCN9A):c.5140G>A (p.Asp1714Asn) rs200733722 0.00003
NM_001365536.1(SCN9A):c.5699A>T (p.Tyr1900Phe) rs201796657 0.00003
NM_001365536.1(SCN9A):c.1603T>G (p.Ser535Ala) rs774903062 0.00002
NM_001365536.1(SCN9A):c.1619G>A (p.Arg540His) rs199748300 0.00002
NM_001365536.1(SCN9A):c.1650C>G (p.Ser550Arg) rs200192044 0.00002
NM_001365536.1(SCN9A):c.2004G>T (p.Arg668Ser) rs200970256 0.00002
NM_001365536.1(SCN9A):c.2166G>C (p.Leu722Phe) rs772492538 0.00002
NM_001365536.1(SCN9A):c.3598C>T (p.Leu1200Phe) rs201233540 0.00002
NM_001365536.1(SCN9A):c.1154T>G (p.Val385Gly) rs202159091 0.00001
NM_001365536.1(SCN9A):c.1208T>C (p.Met403Thr) rs199986805 0.00001
NM_001365536.1(SCN9A):c.1304A>C (p.Glu435Ala) rs201396897 0.00001
NM_001365536.1(SCN9A):c.1309G>A (p.Ala437Thr) rs759299867 0.00001
NM_001365536.1(SCN9A):c.1314+3A>T rs774219473 0.00001
NM_001365536.1(SCN9A):c.1726A>G (p.Ser576Gly) rs202090277 0.00001
NM_001365536.1(SCN9A):c.1792C>T (p.Arg598Cys) rs200065703 0.00001
NM_001365536.1(SCN9A):c.1826C>T (p.Pro609Leu) rs1298846957 0.00001
NM_001365536.1(SCN9A):c.1901G>A (p.Arg634His) rs774510851 0.00001
NM_001365536.1(SCN9A):c.2316C>A (p.Phe772Leu) rs774613581 0.00001
NM_001365536.1(SCN9A):c.2815G>A (p.Ala939Thr) rs1064793264 0.00001
NM_001365536.1(SCN9A):c.2840T>C (p.Val947Ala) rs1395440338 0.00001
NM_001365536.1(SCN9A):c.2930C>G (p.Thr977Arg) rs1369602144 0.00001
NM_001365536.1(SCN9A):c.3448G>A (p.Glu1150Lys) rs367794835 0.00001
NM_001365536.1(SCN9A):c.4163A>G (p.Asn1388Ser) rs923385288 0.00001
NM_001365536.1(SCN9A):c.4358T>C (p.Ile1453Thr) rs1558963758 0.00001
NM_001365536.1(SCN9A):c.4621C>A (p.Gln1541Lys) rs1064796825 0.00001
NM_001365536.1(SCN9A):c.4865G>A (p.Arg1622His) rs1346697903 0.00001
NM_001365536.1(SCN9A):c.4965G>T (p.Met1655Ile) rs200166620 0.00001
NM_001365536.1(SCN9A):c.5164C>T (p.Pro1722Ser) rs201264153 0.00001
NM_001365536.1(SCN9A):c.5207G>C (p.Gly1736Ala) rs776586182 0.00001
NM_001365536.1(SCN9A):c.5497G>A (p.Gly1833Ser) rs201638678 0.00001
NM_001365536.1(SCN9A):c.5563G>A (p.Glu1855Lys) rs876661248 0.00001
NM_001365536.1(SCN9A):c.5615C>T (p.Pro1872Leu) rs879254298 0.00001
NM_001365536.1(SCN9A):c.5954A>G (p.Glu1985Gly) rs755850299 0.00001
NM_001365536.1(SCN9A):c.1022A>G (p.Tyr341Cys) rs374280444
NM_001365536.1(SCN9A):c.1207A>C (p.Met403Leu) rs746956041
NM_001365536.1(SCN9A):c.1288C>A (p.Leu430Ile)
NM_001365536.1(SCN9A):c.1756G>A (p.Gly586Ser) rs754646586
NM_001365536.1(SCN9A):c.1801A>C (p.Asn601His) rs2106483219
NM_001365536.1(SCN9A):c.1937C>G (p.Pro646Arg) rs2106482812
NM_001365536.1(SCN9A):c.1999A>G (p.Lys667Glu) rs775090142
NM_001365536.1(SCN9A):c.2073T>G (p.Ser691Arg) rs1697496394
NM_001365536.1(SCN9A):c.2113G>A (p.Glu705Lys)
NM_001365536.1(SCN9A):c.2152G>T (p.Ala718Ser)
NM_001365536.1(SCN9A):c.2387T>C (p.Ile796Thr) rs2106471480
NM_001365536.1(SCN9A):c.2518-10T>G rs879254177
NM_001365536.1(SCN9A):c.2903T>C (p.Leu968Ser) rs1553486841
NM_001365536.1(SCN9A):c.2923A>T (p.Asn975Tyr) rs2106461476
NM_001365536.1(SCN9A):c.2975T>C (p.Val992Ala) rs1057524814
NM_001365536.1(SCN9A):c.3019C>T (p.Arg1007Cys) rs121908910
NM_001365536.1(SCN9A):c.3169G>A (p.Asp1057Asn) rs370892430
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.3420A>C (p.Glu1140Asp) rs201049193
NM_001365536.1(SCN9A):c.3478G>A (p.Val1160Ile) rs1369161781
NM_001365536.1(SCN9A):c.3632T>C (p.Phe1211Ser) rs2106403732
NM_001365536.1(SCN9A):c.4009A>C (p.Ile1337Leu) rs543167736
NM_001365536.1(SCN9A):c.4073G>A (p.Arg1358Gln) rs200163716
NM_001365536.1(SCN9A):c.4171A>G (p.Asn1391Asp) rs2106387312
NM_001365536.1(SCN9A):c.4198C>A (p.Leu1400Ile) rs2106387233
NM_001365536.1(SCN9A):c.4206+6del rs1375669515
NM_001365536.1(SCN9A):c.4476G>T (p.Lys1492Asn) rs879253974
NM_001365536.1(SCN9A):c.4556T>C (p.Ile1519Thr)
NM_001365536.1(SCN9A):c.4827C>G (p.Phe1609Leu) rs760606370
NM_001365536.1(SCN9A):c.4904T>C (p.Phe1635Ser) rs879254053
NM_001365536.1(SCN9A):c.5086A>T (p.Thr1696Ser) rs879254140
NM_001365536.1(SCN9A):c.5146G>A (p.Asp1716Asn) rs1693375977
NM_001365536.1(SCN9A):c.5251G>C (p.Val1751Leu) rs879253908
NM_001365536.1(SCN9A):c.5269G>A (p.Ala1757Thr)
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.5578C>T (p.Arg1860Cys) rs200494490
NM_001365536.1(SCN9A):c.5588T>C (p.Met1863Thr) rs201561928
NM_001365536.1(SCN9A):c.5738C>G (p.Ser1913Ter)
NM_001365536.1(SCN9A):c.5949C>G (p.Ser1983Arg) rs201640210

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