rs1367226
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1367226(C;C) |
Make rs1367226(C;T) |
Make rs1367226(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 55862405 |
is a | snp |
is | mentioned by |
dbSNP | rs1367226 |
dbSNP (classic) | rs1367226 |
ClinGen | rs1367226 |
ebi | rs1367226 |
HLI | rs1367226 |
Exac | rs1367226 |
Gnomad | rs1367226 |
Varsome | rs1367226 |
LitVar | rs1367226 |
Map | rs1367226 |
PheGenI | rs1367226 |
Biobank | rs1367226 |
1000 genomes | rs1367226 |
hgdp | rs1367226 |
ensembl | rs1367226 |
geneview | rs1367226 |
scholar | rs1367226 |
rs1367226 | |
pharmgkb | rs1367226 |
gwascentral | rs1367226 |
openSNP | rs1367226 |
23andMe | rs1367226 |
SNPshot | rs1367226 |
SNPdbe | rs1367226 |
MSV3d | rs1367226 |
GWAS Ctlg | rs1367226 |
GMAF | 0.2801 |
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 | |
P-val | 4E-8 |
Odds Ratio | NR NR |