rs5916687

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common on affy axiom data

Make rs5916687(A;A)

Make rs5916687(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

4678097

is a	snp
is	mentioned by
dbSNP	rs5916687
dbSNP (classic)	rs5916687
ClinGen	rs5916687
ebi	rs5916687
HLI	rs5916687
Exac	rs5916687
Gnomad	rs5916687
Varsome	rs5916687
LitVar	rs5916687
Map	rs5916687
PheGenI	rs5916687
Biobank	rs5916687
1000 genomes	rs5916687
hgdp	rs5916687
ensembl	rs5916687
geneview	rs5916687
scholar	rs5916687
google	rs5916687
pharmgkb	rs5916687
gwascentral	rs5916687
openSNP	rs5916687
23andMe	rs5916687
SNPshot	rs5916687
SNPdbe	rs5916687
MSV3d	rs5916687
GWAS Ctlg	rs5916687

GMAF

0.1288

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 19734901]
Trait	Amyotrophic lateral sclerosis
Title	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
Risk Allele
P-val	0.000003
Odds Ratio	1.22 [NR]