rs794729216

Orientation

minus

Stabilized

minus

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

Make rs794729216(A;A)

Make rs794729216(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166277134

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs794729216
dbSNP (classic)	rs794729216
ClinGen	rs794729216
ebi	rs794729216
HLI	rs794729216
Exac	rs794729216
Gnomad	rs794729216
Varsome	rs794729216
LitVar	rs794729216
Map	rs794729216
PheGenI	rs794729216
Biobank	rs794729216
1000 genomes	rs794729216
hgdp	rs794729216
ensembl	rs794729216
geneview	rs794729216
scholar	rs794729216
google	rs794729216
pharmgkb	rs794729216
gwascentral	rs794729216
openSNP	rs794729216
23andMe	rs794729216
SNPshot	rs794729216
SNPdbe	rs794729216
MSV3d	rs794729216
GWAS Ctlg	rs794729216

Max Magnitude

0

ClinVar
Risk	rs794729216(A;A)
Alt	rs794729216(A;A)
Reference	Rs794729216(G;G)
Significance	Pathogenic
Disease	Indifference to pain
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	Indifference to pain, congenital, autosomal recessive
Reversed	1
HGVS	NC_000002.11:g.167133644C>T
CLNSRC
CLNACC	RCV000184036.1,