DisGeNET - a database of gene-disease associations

SLC22A23, solute carrier family 22 member 23, 63027

N. diseases: 18; N. variants: 14

Disease: Laryngeal Squamous Cell Carcinoma ×

Variant: rs4959235 ×

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

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs4959235

Entrez Id:	63027
Gene Symbol:	SLC22A23

SLC22A23

CUI:	C0280324
Disease:

Laryngeal Squamous Cell Carcinoma

0.010

GeneticVariation

BEFREE

To understand the association between SNPs in SLC22A23 and LSCC, selected genetic variations (rs4959235, rs6923667, rs9503518) were genotyped.

29703252

2018