DisGeNET - a database of gene-disease associations

Source: ALL

Variant: rs2106261 ×

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:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0004238
Disease:	Atrial Fibrillation

Atrial Fibrillation

0.900

0.929

2009

2019

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0010054
Disease:	Coronary Arteriosclerosis

Coronary Arteriosclerosis

0.010

1.000

2014

2014

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0011849
Disease:	Diabetes Mellitus

Diabetes Mellitus

0.010

1.000

2011

2011

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0010068
Disease:	Coronary heart disease

Coronary heart disease

0.010

1.000

2014

2014

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0003850
Disease:	Arteriosclerosis

Arteriosclerosis

0.010

1.000

2016

2016

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0235480
Disease:	Paroxysmal atrial fibrillation

Paroxysmal atrial fibrillation

0.010

1.000

2018

2018

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0007785
Disease:	Cerebral Infarction

Cerebral Infarction

0.010

1.000

2017

2017

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0004153
Disease:	Atherosclerosis

Atherosclerosis

0.010

1.000

2016

2016

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C1956346
Disease:	Coronary Artery Disease

Coronary Artery Disease

0.010

1.000

2014

2014

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0206698
Disease:	Cholangiocarcinoma

Cholangiocarcinoma

0.010

1.000

2018

2018

dbSNP:

rs2106261

rs2106261

ZFHX3

0.763

0.160

16

73017721

intron variant

C/G;T

snv

CUI:	C0020538
Disease:	Hypertensive disease

Hypertensive disease

0.010

1.000

2011

2011