rs202152511

Orientation

plus

Stabilized

plus

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

Make rs202152511(A;A)

Make rs202152511(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

166277138

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs202152511
dbSNP (classic)	rs202152511
ClinGen	rs202152511
ebi	rs202152511
HLI	rs202152511
Exac	rs202152511
Gnomad	rs202152511
Varsome	rs202152511
LitVar	rs202152511
Map	rs202152511
PheGenI	rs202152511
Biobank	rs202152511
1000 genomes	rs202152511
hgdp	rs202152511
ensembl	rs202152511
geneview	rs202152511
scholar	rs202152511
google	rs202152511
pharmgkb	rs202152511
gwascentral	rs202152511
openSNP	rs202152511
23andMe	rs202152511
SNPshot	rs202152511
SNPdbe	rs202152511
MSV3d	rs202152511
GWAS Ctlg	rs202152511

Max Magnitude

0

ClinVar
Risk	rs202152511(A;A)
Alt	rs202152511(A;A)
Reference	Rs202152511(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.167133648G>A
CLNSRC
CLNACC	RCV000479461.1,