DisGeNET - a database of gene-disease associations

Squamous cell carcinoma of esophagus, C0279626

Variant: rs13042395 ×

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs13042395

SLC52A3

0.040

GeneticVariation

BEFREE

C20orf54 rs13042395 was not associated with ESCC under any genetic model.

30666517

2019

dbSNP:

rs13042395

SLC52A3

0.040

GeneticVariation

BEFREE

The rs13042395 polymorphism in SLC52A3 is associated with regional lymph node metastasis and relapse-free survival in ESCC patients.

27472962

2016

dbSNP:

rs13042395

SLC52A3

0.040

GeneticVariation

BEFREE

In conclusion, C20orf54 rs13042395 polymorphism was significantly associated with decreased ESCC and GCA risk especially for the subjects with under-weight or normal.

26154995

2015

dbSNP:

rs13042395

SLC52A3

0.040

GeneticVariation

BEFREE

We observed that the rs2274223 polymorphism was associated with an increased risk of ESCC in this Korean case-control study and that age may modify the association between the rs13042395 polymorphism and the risk of ESCC.

24152165

2015