DisGeNET - a database of gene-disease associations

CLEC18B, C-type lectin domain family 18 member B, 497190

N. diseases: 12; N. variants: 1

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

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF_EXOME

AF_GENOME

Disease

Disease Class

Score _vda

EI _vda

N. PMIDs

First Ref.

Last Ref.

dbSNP:

rs150933152

1.000

74411734

missense variant

C/T

snv

CUI:	C1836230
Disease:	HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO

HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO

0.700

1.000

2019

dbSNP:

rs150933152

1.000

74411734

missense variant

C/T

snv

CUI:	C0376705
Disease:	Viral Load result

Viral Load result

0.700

1.000

2019

dbSNP:

rs150933152

1.000

74411734

missense variant

C/T

snv

CUI:	C1836231
Disease:	HIV-1, RESISTANCE TO

HIV-1, RESISTANCE TO

0.700

1.000

2019

dbSNP:

rs150933152

1.000

74411734

missense variant

C/T

snv

CUI:	C1836232
Disease:	ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO

ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO

0.700

1.000

2019

dbSNP:

rs150933152

1.000

74411734

missense variant

C/T

snv

CUI:	C1836233
Disease:	AIDS, PROGRESSION TO

AIDS, PROGRESSION TO

0.700

1.000

2019