DisGeNET - a database of gene-disease associations

Stomach Carcinoma, C0699791

Variant: rs104894361 ×

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:

rs104894361

KRAS

0.700

GeneticVariation

UNIPROT

BRAF and KRAS mutations in stomach cancer.

14534542

2003

dbSNP:

rs104894361

KRAS

0.700

GeneticVariation

UNIPROT

Clinicopathologic significance of the K-ras gene codon 12 point mutation in stomach cancer. An analysis of 140 cases.

7773929

1995

dbSNP:

rs104894361

KRAS

0.700

GeneticVariation

UNIPROT

Activated c-Ha-ras oncogene with a guanine to thymine transversion at the twelfth codon in a human stomach cancer cell line.

3034404

1987