rs2154319
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2154319(C;C) |
Make rs2154319(C;T) |
Make rs2154319(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 41280098 |
is a | snp |
is | mentioned by |
dbSNP | rs2154319 |
dbSNP (classic) | rs2154319 |
ClinGen | rs2154319 |
ebi | rs2154319 |
HLI | rs2154319 |
Exac | rs2154319 |
Gnomad | rs2154319 |
Varsome | rs2154319 |
LitVar | rs2154319 |
Map | rs2154319 |
PheGenI | rs2154319 |
Biobank | rs2154319 |
1000 genomes | rs2154319 |
hgdp | rs2154319 |
ensembl | rs2154319 |
geneview | rs2154319 |
scholar | rs2154319 |
rs2154319 | |
pharmgkb | rs2154319 |
gwascentral | rs2154319 |
openSNP | rs2154319 |
23andMe | rs2154319 |
SNPshot | rs2154319 |
SNPdbe | rs2154319 |
MSV3d | rs2154319 |
GWAS Ctlg | rs2154319 |
GMAF | 0.1111 |
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-12 |
Odds Ratio | .03 [NR] unit decrease |