DisGeNET - a database of gene-disease associations

rs11031005, LOC105376607

N. diseases: 5

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

Disease

N. SNPs_d

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF_EXOME

AF_GENOME

Score _vda

EI _vda

N. PMIDs

First Ref.

Last Ref.

Age at menarche

CUI:	C1314691
Disease:	Age at menarche

591

1.000

0.120

11

30204809

intron variant

T/C

snv

0.10

0.700

1.000

2016

2016

Age at menopause

CUI:	C1629609
Disease:	Age at menopause

209

1.000

0.120

11

30204809

intron variant

T/C

snv

0.10

0.700

1.000

2019

2019

Follicle stimulating hormone measurement

CUI:	C0202022
Disease:	Follicle stimulating hormone measurement

12

1.000

0.120

11

30204809

intron variant

T/C

snv

0.10

0.700

1.000

2016

2016

Hormone measurement

CUI:	C0441683
Disease:	Hormone measurement

134

1.000

0.120

11

30204809

intron variant

T/C

snv

0.10

0.700

1.000

2016

2016

Polycystic Ovary Syndrome

CUI:	C0032460
Disease:	Polycystic Ovary Syndrome

363

1.000

0.120

11

30204809

intron variant

T/C

snv

0.10

0.700

1.000

2018

2018