DisGeNET - a database of gene-disease associations

Polycystic Ovary Syndrome, C0032460

Variant: rs11031006 ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs11031006

LOC105376607

0.710

GeneticVariation

BEFREE

The same chr 11p14.1 SNP, rs11031006, in the region of the follicle-stimulating hormone B polypeptide (FSHB) gene strongly associates with PCOS diagnosis and luteinizing hormone levels.

26284813

2015

dbSNP:

rs11031006

LOC105376607

0.710

GeneticVariation

GWASCAT

Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.

26416764

2015

dbSNP:

rs11031006

LOC105376607

0.710

GeneticVariation

GWASCAT

The same chr 11p14.1 SNP, rs11031006, in the region of the follicle-stimulating hormone B polypeptide (FSHB) gene strongly associates with PCOS diagnosis and luteinizing hormone levels.

26284813

2015