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rs2479106

From SNPedia

Orientationplus
Stabilizedplus
Make rs2479106(A;A)
Make rs2479106(A;G)
Make rs2479106(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position123762933
GeneDENND1A
is asnp
is mentioned by
dbSNPrs2479106
ebirs2479106
HLIrs2479106
Exacrs2479106
Varsomers2479106
Maprs2479106
PheGenIrs2479106
hapmaprs2479106
1000 genomesrs2479106
hgdprs2479106
ensemblrs2479106
gopubmedrs2479106
geneviewrs2479106
scholarrs2479106
googlers2479106
pharmgkbrs2479106
gwascentralrs2479106
openSNPrs2479106
23andMers2479106
23andMe allrs2479106
SNP Nexus

SNPshotrs2479106
SNPdbers2479106
MSV3drs2479106
GWAS Ctlgrs2479106
GMAF0.3852
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 8E-19
Odds Ratio 1.3400 [1.26-1.43]


[PMID 22009367] Susceptibility Loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21, and 9q33.3 in a cohort of caucasian women


[PMID 22081247] Family-based analysis of susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3


[PMID 22504079] Association of polycystic ovary syndrome susceptibility single nucleotide polymorphism rs2479106 and PCOS in Caucasian patients with PCOS or hirsutism as referral diagnosis.


[PMID 22547425OA-icon.png] 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


[PMID 22902918] Variants in DENND1A and LHCGR are associated with endometrioid adenocarcinoma

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 5E-10
Odds Ratio 1.35 [NR]


[PMID 25626177] DENND1A gene variants in Bahraini Arab women with polycystic ovary syndrome