DisGeNET - a database of gene-disease associations

Source: BEFREE

Variant: rs9939609 ×

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

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF _EXOME

AF _GENOME

Disease

Score _vda

EI _vda

N_.PMIDs

FirstRef.

LastRef.

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0004096
Disease:	Asthma

Asthma

0.010

1.000

2016

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0043144
Disease:	Wheezing

Wheezing

0.010

1.000

2016

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0596263
Disease:	Carcinogenesis

Carcinogenesis

0.010

1.000

2011

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0003507
Disease:	Aortic Valve Stenosis

Aortic Valve Stenosis

0.010

1.000

2015

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0497327
Disease:	Dementia

Dementia

0.010

1.000

2011

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0011265
Disease:	Presenile dementia

Presenile dementia

0.010

1.000

2011

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0020175
Disease:	Hunger

Hunger

0.010

1.000

2009

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0271638
Disease:	Type 2 diabetes mellitus in obese

Type 2 diabetes mellitus in obese

0.010

1.000

2017

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0027794
Disease:	Neural Tube Defects

Neural Tube Defects

0.010

1.000

2012

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C3159311
Disease:	BORNHOLM EYE DISEASE

BORNHOLM EYE DISEASE

0.010

1.000

2019

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C1960272
Disease:	Latent autoimmune diabetes mellitus in adult

Latent autoimmune diabetes mellitus in adult

0.010

1.000

2019

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C1956346
Disease:	Coronary Artery Disease

Coronary Artery Disease

0.010

< 0.001

2016

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0036341
Disease:	Schizophrenia

Schizophrenia

0.010

1.000

2014

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C2711227
Disease:	Steatohepatitis

Steatohepatitis

0.010

1.000

2014

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C1739108
Disease:	Latent Autoimmune Diabetes in Adults

Latent Autoimmune Diabetes in Adults

0.010

1.000

2019

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0001726
Disease:	Affective Symptoms

Affective Symptoms

0.010

1.000

2018

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0812413
Disease:	Malignant Pleural Mesothelioma

Malignant Pleural Mesothelioma

0.010

1.000

2018

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0342257
Disease:	Complications of Diabetes Mellitus

Complications of Diabetes Mellitus

0.010

< 0.001

2012

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C4552766
Disease:	Miscarriage

Miscarriage

0.010

1.000

2015

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0003125
Disease:	Anorexia Nervosa

Anorexia Nervosa

0.010

1.000

2012

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0007570
Disease:	Celiac Disease

Celiac Disease

0.010

1.000

2015

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0025517
Disease:	Metabolic Diseases

Metabolic Diseases

0.010

1.000

2018

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0002395
Disease:	Alzheimer's Disease

Alzheimer's Disease

0.010

1.000

2011

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0400966
Disease:	Non-alcoholic Fatty Liver Disease

Non-alcoholic Fatty Liver Disease

0.010

1.000

2014

dbSNP:

rs9939609

FTO

0.559

0.720

53786615

intron variant

T/A

snv

0.41

CUI:	C0271650
Disease:	Impaired glucose tolerance

Impaired glucose tolerance

0.010

1.000

2011