rs12478601
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12478601(C;C) |
Make rs12478601(C;T) |
Make rs12478601(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 43494369 |
Gene | THADA |
is a | snp |
is | mentioned by |
dbSNP | rs12478601 |
dbSNP (classic) | rs12478601 |
ClinGen | rs12478601 |
ebi | rs12478601 |
HLI | rs12478601 |
Exac | rs12478601 |
Gnomad | rs12478601 |
Varsome | rs12478601 |
LitVar | rs12478601 |
Map | rs12478601 |
PheGenI | rs12478601 |
Biobank | rs12478601 |
1000 genomes | rs12478601 |
hgdp | rs12478601 |
ensembl | rs12478601 |
geneview | rs12478601 |
scholar | rs12478601 |
rs12478601 | |
pharmgkb | rs12478601 |
gwascentral | rs12478601 |
openSNP | rs12478601 |
23andMe | rs12478601 |
SNPshot | rs12478601 |
SNPdbe | rs12478601 |
MSV3d | rs12478601 |
GWAS Ctlg | rs12478601 |
GMAF | 0.4527 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21151128] |
Trait | |
Title | Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33 |
Risk Allele | C |
P-val | 3E-23 |
Odds Ratio | 1.3900 [1.30-1.49] |
[PMID 22081247] Family-based analysis of susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
[PMID 22547425] Variants in DENND1A Are Associated with Polycystic Ovary Syndrome in Women of European Ancestry.
[PMID 23208300] Genotype-phenotype correlations of PCOS susceptibility SNPs identified by GWAS in a large cohort of Han Chinese women