List of variants in gene combination SCN1A, SCN9A reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.1469G>A (p.Ser490Asn)	rs58022607	0.04393
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu)	rs12478318	0.01480
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu)	rs4369876	0.01322
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser)	rs141268327	0.00496
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val)	rs182650126	0.00270
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg)	rs202084411	0.00190
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg)	rs121908919	0.00176
NM_001365536.1(SCN9A):c.4314C>T (p.Val1438=)	rs188336294	0.00171
NM_001365536.1(SCN9A):c.3051G>C (p.Lys1017Asn)	rs147623238	0.00144
NM_001365536.1(SCN9A):c.3509T>C (p.Ile1170Thr)	rs73019664	0.00128
NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=)	rs111674454	0.00096
NM_001365536.1(SCN9A):c.1326G>A (p.Ala442=)	rs200065104	0.00092
NM_001365536.1(SCN9A):c.1464C>T (p.Leu488=)	rs200682458	0.00058
NM_001365536.1(SCN9A):c.3402G>T (p.Leu1134Phe)	rs200160858	0.00052
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys)	rs199692186	0.00048
NM_001365536.1(SCN9A):c.4495C>A (p.Arg1499=)	rs187558439	0.00019
NM_001365536.1(SCN9A):c.1177C>T (p.Leu393=)	rs184773311	0.00018
NM_001365536.1(SCN9A):c.1110G>A (p.Thr370=)	rs202002028	0.00016
NM_001365536.1(SCN9A):c.3228T>A (p.Gly1076=)	rs200393050	0.00013
NM_001365536.1(SCN9A):c.3207C>T (p.His1069=)	rs200689065	0.00010
NM_001365536.1(SCN9A):c.2165T>C (p.Leu722Ser)	rs187526567	0.00009
NM_001365536.1(SCN9A):c.3975A>G (p.Leu1325=)	rs199988325	0.00009
NM_001365536.1(SCN9A):c.4767C>T (p.Ser1589=)	rs200690956	0.00003
NM_001365536.1(SCN9A):c.1107+7A>G	rs199623041	0.00001
NM_001365536.1(SCN9A):c.1158T>A (p.Ile386=)	rs200963646	0.00001
NM_001365536.1(SCN9A):c.1347T>C (p.Ser449=)	rs201990547	0.00001
NM_001365536.1(SCN9A):c.1566G>A (p.Arg522=)	rs1340370507	0.00001
NM_001365536.1(SCN9A):c.4503+8A>T	rs753899025	0.00001
NM_001365536.1(SCN9A):c.1314+5T>C	rs770452089
NM_001365536.1(SCN9A):c.1974+9_1974+15del	rs771477692
NM_001365536.1(SCN9A):c.2874+11_2874+13delinsTT	rs1553487749
NM_001365536.1(SCN9A):c.3003T>C (p.Tyr1001=)	rs886038521
NM_001365536.1(SCN9A):c.3180T>C (p.Ser1060=)	rs199697334

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