rs10054504
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10054504(C;C) |
Make rs10054504(C;T) |
Make rs10054504(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 32000377 |
Gene | PDZD2 |
is a | snp |
is | mentioned by |
dbSNP | rs10054504 |
dbSNP (classic) | rs10054504 |
ClinGen | rs10054504 |
ebi | rs10054504 |
HLI | rs10054504 |
Exac | rs10054504 |
Gnomad | rs10054504 |
Varsome | rs10054504 |
LitVar | rs10054504 |
Map | rs10054504 |
PheGenI | rs10054504 |
Biobank | rs10054504 |
1000 genomes | rs10054504 |
hgdp | rs10054504 |
ensembl | rs10054504 |
geneview | rs10054504 |
scholar | rs10054504 |
rs10054504 | |
pharmgkb | rs10054504 |
gwascentral | rs10054504 |
openSNP | rs10054504 |
23andMe | rs10054504 |
SNPshot | rs10054504 |
SNPdbe | rs10054504 |
MSV3d | rs10054504 |
GWAS Ctlg | rs10054504 |
GMAF | 0.4155 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23184150] |
Trait | Renal cell carcinoma |
Title | Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer. |
Risk Allele | |
P-val | 8E-7 |
Odds Ratio | 1.37 [1.19-1.58] |
The second strongest signal was provided by rs10054504 which maps to chromosome 5p13.3 (32 000 483 bps; NCBI build 37), within intron 4 of the PDZD2 gene (PDZ domain-containing 2; MIM: 610697), but did not achieve genome-wide significance (P = 7.68 × 10−7; Phet = 0.06, I2 = 57%)[PMID 23184150]
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2d