rs1057518900

Orientation

minus

Stabilized

minus

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

Make rs1057518900(C;T)

Make rs1057518900(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

166284785

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs1057518900
dbSNP (classic)	rs1057518900
ClinGen	rs1057518900
ebi	rs1057518900
HLI	rs1057518900
Exac	rs1057518900
Gnomad	rs1057518900
Varsome	rs1057518900
LitVar	rs1057518900
Map	rs1057518900
PheGenI	rs1057518900
Biobank	rs1057518900
1000 genomes	rs1057518900
hgdp	rs1057518900
ensembl	rs1057518900
geneview	rs1057518900
scholar	rs1057518900
google	rs1057518900
pharmgkb	rs1057518900
gwascentral	rs1057518900
openSNP	rs1057518900
23andMe	rs1057518900
SNPshot	rs1057518900
SNPdbe	rs1057518900
MSV3d	rs1057518900
GWAS Ctlg	rs1057518900

Max Magnitude

0

ClinVar
Risk	rs1057518900(T;T)
Alt	rs1057518900(T;T)
Reference	Rs1057518900(C;C)
Significance	Pathogenic
Disease	Pain insensitivity
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	Pain insensitivity
Reversed	1
HGVS	NC_000002.11:g.167141295G>A
CLNSRC
CLNACC	RCV000414858.1,