rs2059807
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2059807(C;C) |
Make rs2059807(C;T) |
Make rs2059807(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 19 |
Position | 7166098 |
Gene | INSR |
is a | snp |
is | mentioned by |
dbSNP | rs2059807 |
dbSNP (classic) | rs2059807 |
ClinGen | rs2059807 |
ebi | rs2059807 |
HLI | rs2059807 |
Exac | rs2059807 |
Gnomad | rs2059807 |
Varsome | rs2059807 |
LitVar | rs2059807 |
Map | rs2059807 |
PheGenI | rs2059807 |
Biobank | rs2059807 |
1000 genomes | rs2059807 |
hgdp | rs2059807 |
ensembl | rs2059807 |
geneview | rs2059807 |
scholar | rs2059807 |
rs2059807 | |
pharmgkb | rs2059807 |
gwascentral | rs2059807 |
openSNP | rs2059807 |
23andMe | rs2059807 |
SNPshot | rs2059807 |
SNPdbe | rs2059807 |
MSV3d | rs2059807 |
GWAS Ctlg | rs2059807 |
GMAF | 0.449 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21645371] Family association study between INSR gene polymorphisms and PCOS in Han Chinese
[PMID 18194558] A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.
GWAS snp | |
---|---|
PMID | [PMID 22885925] |
Trait | Polycystic ovary syndrome |
Title | Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome. |
Risk Allele | G |
P-val | 1E-8 |
Odds Ratio | 1.14 [NR] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 19
- 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 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d