rs121908920

Orientation

minus

Stabilized

minus

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

Make rs121908920(A;G)

Make rs121908920(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

166311573

Gene

SCN9A

is a	snp
is	mentioned by
dbSNP	rs121908920
dbSNP (classic)	rs121908920
ClinGen	rs121908920
ebi	rs121908920
HLI	rs121908920
Exac	rs121908920
Gnomad	rs121908920
Varsome	rs121908920
LitVar	rs121908920
Map	rs121908920
PheGenI	rs121908920
Biobank	rs121908920
1000 genomes	rs121908920
hgdp	rs121908920
ensembl	rs121908920
geneview	rs121908920
scholar	rs121908920
google	rs121908920
pharmgkb	rs121908920
gwascentral	rs121908920
openSNP	rs121908920
23andMe	rs121908920
SNPshot	rs121908920
SNPdbe	rs121908920
MSV3d	rs121908920
GWAS Ctlg	rs121908920

Max Magnitude

0

OMIM	603415
Desc
Variant	0020
Related	also

ClinVar
Risk	rs121908920(G;G)
Alt	rs121908920(G;G)
Reference	Rs121908920(A;A)
Significance	Pathogenic
Disease	Febrile seizures not specified
Variation	info
Gene	SCN9A
CLNDBN	Febrile seizures, familial, 3b not specified
Reversed	1
HGVS	NC_000002.11:g.167168083T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006740.4, RCV000215091.1,