rs9971637

Orientation

plus

Stabilized

plus

Make rs9971637(A;A)

Make rs9971637(A;G)

Make rs9971637(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

17220805

is a	snp
is	mentioned by
dbSNP	rs9971637
dbSNP (classic)	rs9971637
ClinGen	rs9971637
ebi	rs9971637
HLI	rs9971637
Exac	rs9971637
Gnomad	rs9971637
Varsome	rs9971637
LitVar	rs9971637
Map	rs9971637
PheGenI	rs9971637
Biobank	rs9971637
1000 genomes	rs9971637
hgdp	rs9971637
ensembl	rs9971637
geneview	rs9971637
scholar	rs9971637
google	rs9971637
pharmgkb	rs9971637
gwascentral	rs9971637
openSNP	rs9971637
23andMe	rs9971637
SNPshot	rs9971637
SNPdbe	rs9971637
MSV3d	rs9971637
GWAS Ctlg	rs9971637

GMAF

0.1253

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	0.000002
Odds Ratio	1.48 [NR]