rs121908921

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121908921(A;A)

Make rs121908921(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

166306531

Gene

SCN9A

is a	snp
is	mentioned by
dbSNP	rs121908921
dbSNP (classic)	rs121908921
ClinGen	rs121908921
ebi	rs121908921
HLI	rs121908921
Exac	rs121908921
Gnomad	rs121908921
Varsome	rs121908921
LitVar	rs121908921
Map	rs121908921
PheGenI	rs121908921
Biobank	rs121908921
1000 genomes	rs121908921
hgdp	rs121908921
ensembl	rs121908921
geneview	rs121908921
scholar	rs121908921
google	rs121908921
pharmgkb	rs121908921
gwascentral	rs121908921
openSNP	rs121908921
23andMe	rs121908921
SNPshot	rs121908921
SNPdbe	rs121908921
MSV3d	rs121908921
GWAS Ctlg	rs121908921

Max Magnitude

0

OMIM	603415
Desc
Variant	0021
Related	also

ClinVar
Risk	rs121908921(A;A) rs121908921(T;T)
Alt	rs121908921(A;A) rs121908921(T;T)
Reference	Rs121908921(C;C)
Significance	Pathogenic
Disease	Febrile seizures
Variation	info
Gene	SCN9A
CLNDBN	Febrile seizures, familial, 3b
Reversed	1
HGVS	NC_000002.11:g.167163041G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006741.4,