rs121908914

Orientation

minus

Stabilized

minus

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

Make rs121908914(C;C)

Make rs121908914(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

166204448

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs121908914
dbSNP (classic)	rs121908914
ClinGen	rs121908914
ebi	rs121908914
HLI	rs121908914
Exac	rs121908914
Gnomad	rs121908914
Varsome	rs121908914
LitVar	rs121908914
Map	rs121908914
PheGenI	rs121908914
Biobank	rs121908914
1000 genomes	rs121908914
hgdp	rs121908914
ensembl	rs121908914
geneview	rs121908914
scholar	rs121908914
google	rs121908914
pharmgkb	rs121908914
gwascentral	rs121908914
openSNP	rs121908914
23andMe	rs121908914
SNPshot	rs121908914
SNPdbe	rs121908914
MSV3d	rs121908914
GWAS Ctlg	rs121908914

Max Magnitude

0

OMIM	603415
Desc
Variant	0012
Related	also

ClinVar
Risk	rs121908914(C;C)
Alt	rs121908914(C;C)
Reference	Rs121908914(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.167060958A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006732.3,