ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported by Athena Diagnostics Inc

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Total variants: 26
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HGVS dbSNP
NM_002977.3(SCN9A):c.1109C>T (p.Thr370Met) rs200391162
NM_002977.3(SCN9A):c.1119T>C (p.Ala373=) rs13414203
NM_002977.3(SCN9A):c.1150G>A (p.Val384Ile) rs200973534
NM_002977.3(SCN9A):c.1266A>G (p.Glu422=) rs13402180
NM_002977.3(SCN9A):c.1287T>A (p.Arg429=) rs6747673
NM_002977.3(SCN9A):c.1398C>T (p.Ser466=) rs201531206
NM_002977.3(SCN9A):c.1828C>A (p.Pro610Thr) rs41268673
NM_002977.3(SCN9A):c.1942-3dupT rs35888674
NM_002977.3(SCN9A):c.1964A>G (p.Lys655Arg) rs121908919
NM_002977.3(SCN9A):c.2611G>C (p.Val871Leu) rs1553487882
NM_002977.3(SCN9A):c.2733C>T (p.Arg911=) rs199653503
NM_002977.3(SCN9A):c.2931C>T (p.Leu977=) rs201430964
NM_002977.3(SCN9A):c.3238A>G (p.Ile1080Val) rs202212176
NM_002977.3(SCN9A):c.3328C>T (p.Arg1110Trp) rs190664764
NM_002977.3(SCN9A):c.3448C>T (p.Arg1150Trp) rs6746030
NM_002977.3(SCN9A):c.3476T>C (p.Ile1159Thr) rs73019664
NM_002977.3(SCN9A):c.3505A>G (p.Asn1169Asp) rs750269576
NM_002977.3(SCN9A):c.3734A>G (p.Asn1245Ser) rs141268327
NM_002977.3(SCN9A):c.3769-4A>G rs75230218
NM_002977.3(SCN9A):c.4366-10_4366-7delGTTT rs77944059
NM_002977.3(SCN9A):c.4612T>C (p.Trp1538Arg) rs202084411
NM_002977.3(SCN9A):c.4779G>T (p.Val1593=) rs149207258
NM_002977.3(SCN9A):c.4920C>G (p.Leu1640=)
NM_002977.3(SCN9A):c.4997A>T (p.Asp1666Val) rs1553473210
NM_002977.3(SCN9A):c.5746C>T (p.Leu1916Phe) rs111558968
NM_002977.3(SCN9A):c.5758G>C (p.Asp1920His) rs200410805

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