rs11867479
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11867479(C;C) |
Make rs11867479(C;T) |
Make rs11867479(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 70094066 |
Gene | KCNJ16 |
is a | snp |
is | mentioned by |
dbSNP | rs11867479 |
dbSNP (classic) | rs11867479 |
ClinGen | rs11867479 |
ebi | rs11867479 |
HLI | rs11867479 |
Exac | rs11867479 |
Gnomad | rs11867479 |
Varsome | rs11867479 |
LitVar | rs11867479 |
Map | rs11867479 |
PheGenI | rs11867479 |
Biobank | rs11867479 |
1000 genomes | rs11867479 |
hgdp | rs11867479 |
ensembl | rs11867479 |
geneview | rs11867479 |
scholar | rs11867479 |
rs11867479 | |
pharmgkb | rs11867479 |
gwascentral | rs11867479 |
openSNP | rs11867479 |
23andMe | rs11867479 |
SNPshot | rs11867479 |
SNPdbe | rs11867479 |
MSV3d | rs11867479 |
GWAS Ctlg | rs11867479 |
GMAF | 0.3329 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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-10 |
Odds Ratio | .03 [NR] unit increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 17
- 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 FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d