rs1712790
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1712790(C;C) |
Make rs1712790(C;T) |
Make rs1712790(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 114750747 |
Gene | NXPE2 |
is a | snp |
is | mentioned by |
dbSNP | rs1712790 |
dbSNP (classic) | rs1712790 |
ClinGen | rs1712790 |
ebi | rs1712790 |
HLI | rs1712790 |
Exac | rs1712790 |
Gnomad | rs1712790 |
Varsome | rs1712790 |
LitVar | rs1712790 |
Map | rs1712790 |
PheGenI | rs1712790 |
Biobank | rs1712790 |
1000 genomes | rs1712790 |
hgdp | rs1712790 |
ensembl | rs1712790 |
geneview | rs1712790 |
scholar | rs1712790 |
rs1712790 | |
pharmgkb | rs1712790 |
gwascentral | rs1712790 |
openSNP | rs1712790 |
23andMe | rs1712790 |
SNPshot | rs1712790 |
SNPdbe | rs1712790 |
MSV3d | rs1712790 |
GWAS Ctlg | rs1712790 |
GMAF | 0.4063 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs1712790 |
PubMedID | [PMID 17903292] |
Condition | Urinary albumin excretion |
Gene | FAM55B |
Risk Allele | |
pValue | 2.00E-006 |
OR | NA |
95% CI |