rs11575580
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs11575580(C;T) |
Make rs11575580(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 9 |
Position | 34660867 |
Gene | IL11RA |
is a | snp |
is | mentioned by |
dbSNP | rs11575580 |
dbSNP (classic) | rs11575580 |
ClinGen | rs11575580 |
ebi | rs11575580 |
HLI | rs11575580 |
Exac | rs11575580 |
Gnomad | rs11575580 |
Varsome | rs11575580 |
LitVar | rs11575580 |
Map | rs11575580 |
PheGenI | rs11575580 |
Biobank | rs11575580 |
1000 genomes | rs11575580 |
hgdp | rs11575580 |
ensembl | rs11575580 |
geneview | rs11575580 |
scholar | rs11575580 |
rs11575580 | |
pharmgkb | rs11575580 |
gwascentral | rs11575580 |
openSNP | rs11575580 |
23andMe | rs11575580 |
SNPshot | rs11575580 |
SNPdbe | rs11575580 |
MSV3d | rs11575580 |
GWAS Ctlg | rs11575580 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.