rs2405657

Orientation

plus

Stabilized

plus

Make rs2405657(A;A)

Make rs2405657(A;G)

Make rs2405657(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

97811564

is a	snp
is	mentioned by
dbSNP	rs2405657
dbSNP (classic)	rs2405657
ClinGen	rs2405657
ebi	rs2405657
HLI	rs2405657
Exac	rs2405657
Gnomad	rs2405657
Varsome	rs2405657
LitVar	rs2405657
Map	rs2405657
PheGenI	rs2405657
Biobank	rs2405657
1000 genomes	rs2405657
hgdp	rs2405657
ensembl	rs2405657
geneview	rs2405657
scholar	rs2405657
google	rs2405657
pharmgkb	rs2405657
gwascentral	rs2405657
openSNP	rs2405657
23andMe	rs2405657
SNPshot	rs2405657
SNPdbe	rs2405657
MSV3d	rs2405657
GWAS Ctlg	rs2405657

GMAF

0.4096

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	1.19 [NR]