rs200972952

Orientation

plus

Stabilized

plus

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

Make rs200972952(A;A)

Make rs200972952(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

166306951

Gene

SCN9A

is a	snp
is	mentioned by
dbSNP	rs200972952
dbSNP (classic)	rs200972952
ClinGen	rs200972952
ebi	rs200972952
HLI	rs200972952
Exac	rs200972952
Gnomad	rs200972952
Varsome	rs200972952
LitVar	rs200972952
Map	rs200972952
PheGenI	rs200972952
Biobank	rs200972952
1000 genomes	rs200972952
hgdp	rs200972952
ensembl	rs200972952
geneview	rs200972952
scholar	rs200972952
google	rs200972952
pharmgkb	rs200972952
gwascentral	rs200972952
openSNP	rs200972952
23andMe	rs200972952
SNPshot	rs200972952
SNPdbe	rs200972952
MSV3d	rs200972952
GWAS Ctlg	rs200972952

Max Magnitude

0

ClinVar
Risk	rs200972952(A;A) rs200972952(T;T)
Alt	rs200972952(A;A) rs200972952(T;T)
Reference	Rs200972952(G;G)
Significance	Pathogenic
Disease	Pain insensitivity
Variation	info
Gene	SCN9A
CLNDBN	Pain insensitivity
Reversed	0
HGVS	NC_000002.11:g.167163461G>A
CLNSRC
CLNACC	RCV000415348.1,