DisGeNET - a database of gene-disease associations

FGFR2, fibroblast growth factor receptor 2, 2263

N. diseases: 731; N. variants: 141

Disease: Stomach Neoplasms ×

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:

rs1057519044

rs1057519044

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0038356
Disease:

Stomach Neoplasms

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs121913478

rs121913478

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0038356
Disease:

Stomach Neoplasms

C

0.700

CausalMutation

CLINVAR

dbSNP:

rs121918487

rs121918487

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0038356
Disease:

Stomach Neoplasms

T

0.700

CausalMutation

CLINVAR

dbSNP:

rs121918491

rs121918491

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0038356
Disease:

Stomach Neoplasms

T

0.700

CausalMutation

CLINVAR

dbSNP:

rs121918505

rs121918505

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0038356
Disease:

Stomach Neoplasms

G

0.700

CausalMutation

CLINVAR

dbSNP:

rs1434545235

rs1434545235

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0038356
Disease:

Stomach Neoplasms

C

0.700

CausalMutation

CLINVAR

dbSNP:

rs1554927408

rs1554927408

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0038356
Disease:

Stomach Neoplasms

T

0.700

CausalMutation

CLINVAR

dbSNP:

rs77543610

rs77543610

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0038356
Disease:

Stomach Neoplasms

C

0.700

CausalMutation

CLINVAR

dbSNP:

rs79184941

rs79184941

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0038356
Disease:

Stomach Neoplasms

C

0.700

CausalMutation

CLINVAR