rs746241591

Orientation

plus

Stabilized

plus

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

Make rs746241591(A;A)

Make rs746241591(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

166204359

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs746241591
dbSNP (classic)	rs746241591
ClinGen	rs746241591
ebi	rs746241591
HLI	rs746241591
Exac	rs746241591
Gnomad	rs746241591
Varsome	rs746241591
LitVar	rs746241591
Map	rs746241591
PheGenI	rs746241591
Biobank	rs746241591
1000 genomes	rs746241591
hgdp	rs746241591
ensembl	rs746241591
geneview	rs746241591
scholar	rs746241591
google	rs746241591
pharmgkb	rs746241591
gwascentral	rs746241591
openSNP	rs746241591
23andMe	rs746241591
SNPshot	rs746241591
SNPdbe	rs746241591
MSV3d	rs746241591
GWAS Ctlg	rs746241591

Max Magnitude

0

ClinVar
Risk	rs746241591(A;A)
Alt	rs746241591(A;A)
Reference	Rs746241591(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.167060869C>A
CLNSRC
CLNACC	RCV000236300.1,