rs12680546

Orientation

plus

Stabilized

plus

Make rs12680546(A;A)

Make rs12680546(A;G)

Make rs12680546(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

135859496

is a	snp
is	mentioned by
dbSNP	rs12680546
dbSNP (classic)	rs12680546
ClinGen	rs12680546
ebi	rs12680546
HLI	rs12680546
Exac	rs12680546
Gnomad	rs12680546
Varsome	rs12680546
LitVar	rs12680546
Map	rs12680546
PheGenI	rs12680546
Biobank	rs12680546
1000 genomes	rs12680546
hgdp	rs12680546
ensembl	rs12680546
geneview	rs12680546
scholar	rs12680546
google	rs12680546
pharmgkb	rs12680546
gwascentral	rs12680546
openSNP	rs12680546
23andMe	rs12680546
SNPshot	rs12680546
SNPdbe	rs12680546
MSV3d	rs12680546
GWAS Ctlg	rs12680546

GMAF

0.1671

Max Magnitude

0

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

GWAS
SNP	rs12680546
PubMedID	[PMID 17362836]
Condition	Amyotrophic lateral sclerosis
Gene	Intergenic
Risk Allele
pValue	3.00E-006
OR	1.67
95% CI	1.25-2.00

[PMID 17052657] Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.

[PMID 19740415] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis.