rs121908915

Orientation

minus

Stabilized

minus

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

Make rs121908915(C;T)

Make rs121908915(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

166204439

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs121908915
dbSNP (classic)	rs121908915
ClinGen	rs121908915
ebi	rs121908915
HLI	rs121908915
Exac	rs121908915
Gnomad	rs121908915
Varsome	rs121908915
LitVar	rs121908915
Map	rs121908915
PheGenI	rs121908915
Biobank	rs121908915
1000 genomes	rs121908915
hgdp	rs121908915
ensembl	rs121908915
geneview	rs121908915
scholar	rs121908915
google	rs121908915
pharmgkb	rs121908915
gwascentral	rs121908915
openSNP	rs121908915
23andMe	rs121908915
SNPshot	rs121908915
SNPdbe	rs121908915
MSV3d	rs121908915
GWAS Ctlg	rs121908915

Max Magnitude

0

OMIM	603415
Desc
Variant	0013
Related	also

ClinVar
Risk	rs121908915(T;T)
Alt	rs121908915(T;T)
Reference	Rs121908915(C;C)
Significance	Pathogenic
Disease	Paroxysmal extreme pain disorder
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	Paroxysmal extreme pain disorder
Reversed	1
HGVS	NC_000002.11:g.167060949G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006733.3,