List of variants in gene combination SCN1A, SCN9A reported as likely benign for Small fiber neuropathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 37

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.3362G>A (p.Arg1121Gln)	rs74401238	0.02210
NM_001365536.1(SCN9A):c.*377C>G	rs115464654	0.00575
NM_001365536.1(SCN9A):c.*2323G>T	rs142172527	0.00561
NM_001365536.1(SCN9A):c.2517+6C>T	rs145316463	0.00460
NM_001365536.1(SCN9A):c.1398C>T (p.Ser466=)	rs201531206	0.00386
NM_001365536.1(SCN9A):c.*2212T>C	rs200750861	0.00201
NM_001365536.1(SCN9A):c.*785C>T	rs181229506	0.00108
NM_001365536.1(SCN9A):c.*2191G>A	rs201184093	0.00091
NM_001365536.1(SCN9A):c.3020G>A (p.Arg1007His)	rs188145203	0.00077
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile)	rs149346064	0.00061
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.3801T>C (p.Asp1267=)	rs202047865	0.00043
NM_001365536.1(SCN9A):c.4399-14G>T	rs112927502	0.00038
NM_001365536.1(SCN9A):c.3684T>C (p.Tyr1228=)	rs144941725	0.00035
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.3472+14T>C	rs201979079	0.00017
NM_001365536.1(SCN9A):c.*2078C>T	rs548072061	0.00014
NM_001365536.1(SCN9A):c.2875-5del	rs774840081	0.00011
NM_001365536.1(SCN9A):c.2875-6A>G	rs760470229	0.00011
NM_001365536.1(SCN9A):c.2165T>C (p.Leu722Ser)	rs187526567	0.00009
NM_001365536.1(SCN9A):c.5711G>A (p.Arg1904His)	rs79805025	0.00009
NM_001365536.1(SCN9A):c.*125C>T	rs200465050	0.00004
NM_001365536.1(SCN9A):c.1619G>A (p.Arg540His)	rs199748300	0.00002
NM_001365536.1(SCN9A):c.*217G>A	rs200625860	0.00001
NM_001365536.1(SCN9A):c.*2721C>G	rs199595958	0.00001
NM_001365536.1(SCN9A):c.*669A>G	rs538508619	0.00001
NM_001365536.1(SCN9A):c.1208T>C (p.Met403Thr)	rs199986805	0.00001
NM_001365536.1(SCN9A):c.1482G>T (p.Lys494Asn)	rs777699798	0.00001
NM_001365536.1(SCN9A):c.2852T>C (p.Val951Ala)	rs201890077	0.00001
NM_001365536.1(SCN9A):c.*1434dup	rs199505193
NM_001365536.1(SCN9A):c.1605_1606del	rs200091138
NM_001365536.1(SCN9A):c.1960_1962dup	rs202073550
NM_001365536.1(SCN9A):c.*920T>A	rs201424899
NM_001365536.1(SCN9A):c.1603-14dup	rs200430382
NM_001365536.1(SCN9A):c.1975-3del	rs35888674

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