rs10007590
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10007590(A;A) |
Make rs10007590(A;G) |
Make rs10007590(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 88995984 |
Gene | FAM13A |
is a | snp |
is | mentioned by |
dbSNP | rs10007590 |
dbSNP (classic) | rs10007590 |
ClinGen | rs10007590 |
ebi | rs10007590 |
HLI | rs10007590 |
Exac | rs10007590 |
Gnomad | rs10007590 |
Varsome | rs10007590 |
LitVar | rs10007590 |
Map | rs10007590 |
PheGenI | rs10007590 |
Biobank | rs10007590 |
1000 genomes | rs10007590 |
hgdp | rs10007590 |
ensembl | rs10007590 |
geneview | rs10007590 |
scholar | rs10007590 |
rs10007590 | |
pharmgkb | rs10007590 |
gwascentral | rs10007590 |
openSNP | rs10007590 |
23andMe | rs10007590 |
SNPshot | rs10007590 |
SNPdbe | rs10007590 |
MSV3d | rs10007590 |
GWAS Ctlg | rs10007590 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23891779] Association of FAM13A polymorphisms with COPD and COPD-related phenotypes in Han Chinese