rs121908913

Orientation

minus

Stabilized

minus

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

Make rs121908913(G;T)

Make rs121908913(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

166228969

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs121908913
dbSNP (classic)	rs121908913
ClinGen	rs121908913
ebi	rs121908913
HLI	rs121908913
Exac	rs121908913
Gnomad	rs121908913
Varsome	rs121908913
LitVar	rs121908913
Map	rs121908913
PheGenI	rs121908913
Biobank	rs121908913
1000 genomes	rs121908913
hgdp	rs121908913
ensembl	rs121908913
geneview	rs121908913
scholar	rs121908913
google	rs121908913
pharmgkb	rs121908913
gwascentral	rs121908913
openSNP	rs121908913
23andMe	rs121908913
SNPshot	rs121908913
SNPdbe	rs121908913
MSV3d	rs121908913
GWAS Ctlg	rs121908913

Max Magnitude

0

OMIM	603415
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121908913(T;T)
Alt	rs121908913(T;T)
Reference	Rs121908913(G;G)
Significance	Pathogenic
Disease	Paroxysmal extreme pain disorder
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	Paroxysmal extreme pain disorder
Reversed	1
HGVS	NC_000002.11:g.167085479C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006731.3,