rs770416478

Orientation

plus

Stabilized

plus

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

Make rs770416478(C;G)

Make rs770416478(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

166199247

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs770416478
dbSNP (classic)	rs770416478
ClinGen	rs770416478
ebi	rs770416478
HLI	rs770416478
Exac	rs770416478
Gnomad	rs770416478
Varsome	rs770416478
LitVar	rs770416478
Map	rs770416478
PheGenI	rs770416478
Biobank	rs770416478
1000 genomes	rs770416478
hgdp	rs770416478
ensembl	rs770416478
geneview	rs770416478
scholar	rs770416478
google	rs770416478
pharmgkb	rs770416478
gwascentral	rs770416478
openSNP	rs770416478
23andMe	rs770416478
SNPshot	rs770416478
SNPdbe	rs770416478
MSV3d	rs770416478
GWAS Ctlg	rs770416478

Max Magnitude

0

ClinVar
Risk	rs770416478(A;A) rs770416478(G;G)
Alt	rs770416478(A;A) rs770416478(G;G)
Reference	Rs770416478(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.167055757C>A
CLNSRC
CLNACC	RCV000236372.1,