rs1057518162

Orientation

minus

Stabilized

minus

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

Make rs1057518162(A;A)

Make rs1057518162(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

166280559

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs1057518162
dbSNP (classic)	rs1057518162
ClinGen	rs1057518162
ebi	rs1057518162
HLI	rs1057518162
Exac	rs1057518162
Gnomad	rs1057518162
Varsome	rs1057518162
LitVar	rs1057518162
Map	rs1057518162
PheGenI	rs1057518162
Biobank	rs1057518162
1000 genomes	rs1057518162
hgdp	rs1057518162
ensembl	rs1057518162
geneview	rs1057518162
scholar	rs1057518162
google	rs1057518162
pharmgkb	rs1057518162
gwascentral	rs1057518162
openSNP	rs1057518162
23andMe	rs1057518162
SNPshot	rs1057518162
SNPdbe	rs1057518162
MSV3d	rs1057518162
GWAS Ctlg	rs1057518162

Max Magnitude

0

ClinVar
Risk	rs1057518162(A;A)
Alt	rs1057518162(A;A)
Reference	Rs1057518162(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.167137069C>T
CLNSRC
CLNACC	RCV000414021.1,