Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913528
rs121913528
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014

dbSNP: rs121913528
rs121913528
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
T 0.700 GeneticVariation CLINVAR Effect of simvastatin on cetuximab resistance in human colorectal cancer with KRAS mutations. 21398618

2011

dbSNP: rs121913528
rs121913528
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT BRAF and KRAS mutations in stomach cancer. 14534542

2003

dbSNP: rs121913528
rs121913528
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
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: rs121913528
rs121913528
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
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

dbSNP: rs121913528
rs121913528
CUI: C0424939
Disease: Learning difficulties
Learning difficulties
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913528
rs121913528
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913528
rs121913528
CUI: C1842881
Disease: Dilated aortic root
Dilated aortic root
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913528
rs121913528
CUI: C0349588
Disease: Short stature
Short stature
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913528
rs121913528
CUI: C0575158
Disease: Kyphoscoliosis deformity of spine
Kyphoscoliosis deformity of spine
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913528
rs121913528
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913528
rs121913528
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913528
rs121913528
CUI: C0521525
Disease: Short neck
Short neck
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913528
rs121913528
CUI: C0151699
Disease: Intracranial Hemorrhage
Intracranial Hemorrhage
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913528
rs121913528
BLADDER CANCER, TRANSITIONAL CELL, SOMATIC
T 0.700 CausalMutation CLINVAR