rs4657616
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4657616(A;A) |
Make rs4657616(A;G) |
Make rs4657616(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 159001296 |
Gene | IFI16, POP3, PYHIN1 |
is a | snp |
is | mentioned by |
dbSNP | rs4657616 |
dbSNP (classic) | rs4657616 |
ClinGen | rs4657616 |
ebi | rs4657616 |
HLI | rs4657616 |
Exac | rs4657616 |
Gnomad | rs4657616 |
Varsome | rs4657616 |
LitVar | rs4657616 |
Map | rs4657616 |
PheGenI | rs4657616 |
Biobank | rs4657616 |
1000 genomes | rs4657616 |
hgdp | rs4657616 |
ensembl | rs4657616 |
geneview | rs4657616 |
scholar | rs4657616 |
rs4657616 | |
pharmgkb | rs4657616 |
gwascentral | rs4657616 |
openSNP | rs4657616 |
23andMe | rs4657616 |
SNPshot | rs4657616 |
SNPdbe | rs4657616 |
MSV3d | rs4657616 |
GWAS Ctlg | rs4657616 |
GMAF | 0.348 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23263863] |
Trait | Hematology traits |
Title | GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. |
Risk Allele | G |
P-val | 5E-47 |
Odds Ratio | .06 [0.053-0.07] unit increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- 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 v2c
- On chip Ancestry v2d