DisGeNET - a database of gene-disease associations

rs333947, CSF1

N. diseases: 7

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.

White Blood Cell Count procedure

CUI:	C0023508
Disease:	White Blood Cell Count procedure

1322

1

109928142

intron variant

G/A

snv

0.13

0.700

1.000

2016

2019

Aspartate aminotransferase measurement

CUI:	C0201899
Disease:	Aspartate aminotransferase measurement

76

1

109928142

intron variant

G/A

snv

0.13

0.700

1.000

2018

2018

Blood Protein Measurement

CUI:	C2985280
Disease:	Blood Protein Measurement

2575

1

109928142

intron variant

G/A

snv

0.13

0.700

1.000

2018

2018

Creatine kinase measurement

CUI:	C0201973
Disease:	Creatine kinase measurement

51

1

109928142

intron variant

G/A

snv

0.13

0.700

1.000

2018

2018

High density lipoprotein measurement

CUI:	C0392885
Disease:	High density lipoprotein measurement

1440

1

109928142

intron variant

G/A

snv

0.13

0.700

1.000

2018

2018

Monocyte count procedure

CUI:	C0200637
Disease:	Monocyte count procedure

296

1

109928142

intron variant

G/A

snv

0.13

0.700

1.000

2016

2016

Monocyte count result

CUI:	C0750880
Disease:	Monocyte count result

296

1

109928142

intron variant

G/A

snv

0.13

0.700

1.000

2016

2016