DisGeNET - a database of gene-disease associations

Gastroesophageal reflux disease, C0017168

Variant: rs4965272 ×

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:

rs4965272

rs4965272

ADAMTS17

0.010

GeneticVariation

BEFREE

Concerning the rs4965272, only the GG genotype was significantly associated with GERD (<i>P</i>= 0.035; OR, 3.42; 95% CI, 1.06-11.05).

2019