rs494459
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs494459(A;A) |
Make rs494459(A;G) |
Make rs494459(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 11 |
Position | 118703966 |
Gene | LOC105369519 |
is a | snp |
is | mentioned by |
dbSNP | rs494459 |
dbSNP (classic) | rs494459 |
ClinGen | rs494459 |
ebi | rs494459 |
HLI | rs494459 |
Exac | rs494459 |
Gnomad | rs494459 |
Varsome | rs494459 |
LitVar | rs494459 |
Map | rs494459 |
PheGenI | rs494459 |
Biobank | rs494459 |
1000 genomes | rs494459 |
hgdp | rs494459 |
ensembl | rs494459 |
geneview | rs494459 |
scholar | rs494459 |
rs494459 | |
pharmgkb | rs494459 |
gwascentral | rs494459 |
openSNP | rs494459 |
23andMe | rs494459 |
SNPshot | rs494459 |
SNPdbe | rs494459 |
MSV3d | rs494459 |
GWAS Ctlg | rs494459 |
GMAF | 0.405 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | Height |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | T |
P-val | 2E-8 |
Odds Ratio | .02 [NR] unit increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d