rs13405728

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs13405728(A;G)

Make rs13405728(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48751020

Gene	LHCGR, STON1-GTF2A1L

is a	snp
is	mentioned by
dbSNP	rs13405728
dbSNP (classic)	rs13405728
ClinGen	rs13405728
ebi	rs13405728
HLI	rs13405728
Exac	rs13405728
Gnomad	rs13405728
Varsome	rs13405728
LitVar	rs13405728
Map	rs13405728
PheGenI	rs13405728
Biobank	rs13405728
1000 genomes	rs13405728
hgdp	rs13405728
ensembl	rs13405728
geneview	rs13405728
scholar	rs13405728
google	rs13405728
pharmgkb	rs13405728
gwascentral	rs13405728
openSNP	rs13405728
23andMe	rs13405728
SNPshot	rs13405728
SNPdbe	rs13405728
MSV3d	rs13405728
GWAS Ctlg	rs13405728

GMAF

0.2048

Max Magnitude

0

?	(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	A
P-val	8E-21
Odds Ratio	1.4100 [1.30-1.49]

[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 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

[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	A
P-val	4E-9
Odds Ratio	1.35 [NR]

[PMID 29727258] Association study between variants in LHCGR DENND1A and THADA with preeclampsia risk in Han Chinese populations.