{{Rsnum
|rsid=13429458
|Gene=THADA
|Chromosome=2
|position=43411699
|Orientation=plus
|GMAF=0.1713
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=THADA
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 83.2 | 15.0 | 1.8
| HCB | 59.9 | 35.0 | 5.1
| JPT | 50.9 | 36.6 | 12.5
| YRI | 65.3 | 32.7 | 2.0
| ASW | 73.7 | 26.3 | 0.0
| CHB | 59.9 | 35.0 | 5.1
| CHD | 65.1 | 33.9 | 0.9
| GIH | 74.3 | 23.8 | 2.0
| LWK | 54.5 | 43.6 | 1.8
| MEX | 77.6 | 22.4 | 0.0
| MKK | 60.3 | 35.3 | 4.5
| TSI | 70.6 | 28.4 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21151128
|Trait=None
|Title=Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33
|RiskAllele=A
|Pval=2E-23
|OR=1.4900
|ORtxt=[1.39-1.61]
}}

{{PMID Auto
|PMID=22009367
|Title=Susceptibility Loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21, and 9q33.3 in a cohort of caucasian women
}}

{{PMID Auto
|PMID=22081247
|Title=Family-based analysis of susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
}}

{{PMID Auto
|PMID=22504079
|Title=Association of polycystic ovary syndrome susceptibility single nucleotide polymorphism rs2479106 and PCOS in Caucasian patients with PCOS or hirsutism as referral diagnosis.
}}

{{PMID Auto
|PMID=22547425
|Title=Variants in DENND1A Are Associated with Polycystic Ovary Syndrome in Women of European Ancestry.
|OA=1
}}

{{PMID Auto
|PMID=23208300
|Title=Genotype-phenotype correlations of PCOS susceptibility SNPs identified by GWAS in a large cohort of Han Chinese women
}}

{{PMID Auto
|PMID=22902918
|Title=Variants in DENND1A and LHCGR are associated with endometrioid adenocarcinoma
}}

{{PMID Auto GWAS
  |PMID=22952603
  |Trait=Response to amphetamines
  |Title=Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13).
  |RiskAllele=
  |Pval=6E-6
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{PMID Auto GWAS
  |PMID=22885925
  |Trait=Polycystic ovary syndrome
  |Title=Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome.
  |RiskAllele=A
  |Pval=4E-13
  |OR=1.49
  |ORtxt=[NR]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}