rs121908911

Orientation

minus

Stabilized

minus

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

Make rs121908911(A;A)

Make rs121908911(A;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

166228971

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs121908911
dbSNP (classic)	rs121908911
ClinGen	rs121908911
ebi	rs121908911
HLI	rs121908911
Exac	rs121908911
Gnomad	rs121908911
Varsome	rs121908911
LitVar	rs121908911
Map	rs121908911
PheGenI	rs121908911
Biobank	rs121908911
1000 genomes	rs121908911
hgdp	rs121908911
ensembl	rs121908911
geneview	rs121908911
scholar	rs121908911
google	rs121908911
pharmgkb	rs121908911
gwascentral	rs121908911
openSNP	rs121908911
23andMe	rs121908911
SNPshot	rs121908911
SNPdbe	rs121908911
MSV3d	rs121908911
GWAS Ctlg	rs121908911

Max Magnitude

0

OMIM	603415
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121908911(A;A)
Alt	rs121908911(A;A)
Reference	Rs121908911(T;T)
Significance	Pathogenic
Disease	Paroxysmal extreme pain disorder
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	Paroxysmal extreme pain disorder
Reversed	1
HGVS	NC_000002.11:g.167085481A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006729.3,