rs16984239
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16984239(A;A) |
Make rs16984239(A;C) |
Make rs16984239(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 18053180 |
is a | snp |
is | mentioned by |
dbSNP | rs16984239 |
dbSNP (classic) | rs16984239 |
ClinGen | rs16984239 |
ebi | rs16984239 |
HLI | rs16984239 |
Exac | rs16984239 |
Gnomad | rs16984239 |
Varsome | rs16984239 |
LitVar | rs16984239 |
Map | rs16984239 |
PheGenI | rs16984239 |
Biobank | rs16984239 |
1000 genomes | rs16984239 |
hgdp | rs16984239 |
ensembl | rs16984239 |
geneview | rs16984239 |
scholar | rs16984239 |
rs16984239 | |
pharmgkb | rs16984239 |
gwascentral | rs16984239 |
openSNP | rs16984239 |
23andMe | rs16984239 |
SNPshot | rs16984239 |
SNPdbe | rs16984239 |
MSV3d | rs16984239 |
GWAS Ctlg | rs16984239 |
GMAF | 0.1694 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs16984239 |
PubMedID | [PMID 17362836] |
Condition | Amyotrophic lateral sclerosis |
Gene | Intergenic |
Risk Allele | |
pValue | 2.00E-006 |
OR | 2.1 |
95% CI | 1.50-3.00 |
[PMID 19740415] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis
[PMID 20823317] is-rSNP: a novel technique for in silico regulatory SNP detection.