List of variants in gene SCN1A reported as benign for not specified

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_001165963.4(SCN1A):c.2292T>C (p.Val764=)	rs6432860	0.73885
NM_001165963.4(SCN1A):c.965-21C>T	rs994399	0.66184
NM_001165963.4(SCN1A):c.1212A>G (p.Val404=)	rs7580482	0.66162
NM_001165963.4(SCN1A):c.2176+17A>G	rs59251406	0.03846
NM_001165963.4(SCN1A):c.345T>C (p.Asn115=)	rs61741123	0.03029
NM_001165963.4(SCN1A):c.1662+9C>A	rs7559148	0.02030
NM_001165963.4(SCN1A):c.384-20G>C	rs192956852	0.00635
NM_001165963.4(SCN1A):c.1131A>C (p.Arg377=)	rs114137271	0.00322
NM_001165963.4(SCN1A):c.2889T>C (p.Ala963=)	rs144679294	0.00321
NM_001165963.4(SCN1A):c.1377+10C>T	rs56112036	0.00248
NM_001165963.4(SCN1A):c.1625G>A (p.Arg542Gln)	rs121918817	0.00154
NM_001165963.4(SCN1A):c.68C>T (p.Ala23Val)	rs139397227	0.00138
NM_001165963.4(SCN1A):c.1811G>A (p.Arg604His)	rs121918769	0.00087
NM_001165963.4(SCN1A):c.2421C>T (p.Phe807=)	rs145101180	0.00062
NM_001165963.4(SCN1A):c.694+10A>G	rs373417440	0.00019
NM_001165963.4(SCN1A):c.1378-3T>C	rs150964803	0.00016
NM_001165963.4(SCN1A):c.1410C>T (p.Ser470=)	rs142571794	0.00015
NM_001165963.4(SCN1A):c.579C>T (p.Leu193=)	rs116478064	0.00014
NM_001165963.4(SCN1A):c.1680T>C (p.Arg560=)	rs145662732	0.00011
NM_001165963.4(SCN1A):c.333A>G (p.Leu111=)	rs201592683	0.00006
NM_001165963.4(SCN1A):c.1065T>C (p.Gly355=)	rs757535449	0.00003
NM_001165963.4(SCN1A):c.1663-3T>C	rs766418091	0.00001
NM_001165963.4(SCN1A):c.2044-20A>G	rs777660738	0.00001
NM_001165963.4(SCN1A):c.265-4A>G	rs776470979	0.00001
NM_001165963.4(SCN1A):c.1171-10_1171-9del	rs372840031
NM_001165963.4(SCN1A):c.1539A>G (p.Glu513=)	rs587781144
NM_001165963.4(SCN1A):c.2044-5del	rs549232924
NM_001165963.4(SCN1A):c.2044-5dup	rs549232924
NM_001165963.4(SCN1A):c.2177-11dup	rs11394960
NM_001165963.4(SCN1A):c.2292T>A (p.Val764=)	rs6432860
NM_001165963.4(SCN1A):c.2416-4T>G	rs398123587
NM_001165963.4(SCN1A):c.2589+18_2589+19del	rs3032638
NM_001165963.4(SCN1A):c.602+6_602+7dup	rs577627288

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