rs121913528, KRAS

N. diseases: 12
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968 2014
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
0.700 GeneticVariation CLINVAR Effect of simvastatin on cetuximab resistance in human colorectal cancer with KRAS mutations. 21398618 2011
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
0.700 GeneticVariation UNIPROT BRAF and KRAS mutations in stomach cancer. 14534542 2003
Stomach Carcinoma
CUI: C0699791
Disease: 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
Stomach Carcinoma
CUI: C0699791
Disease: 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
Learning difficulties
CUI: C0424939
Disease: Learning difficulties
0.700 GeneticVariation CLINVAR
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
0.700 GeneticVariation CLINVAR
Dilated aortic root
CUI: C1842881
Disease: Dilated aortic root
0.700 GeneticVariation CLINVAR
Short stature
CUI: C0349588
Disease: Short stature
0.700 GeneticVariation CLINVAR
Kyphoscoliosis deformity of spine
CUI: C0575158
Disease: Kyphoscoliosis deformity of spine
0.700 GeneticVariation CLINVAR
Delayed female puberty
CUI: C0271618
Disease: Delayed female puberty
0.700 GeneticVariation CLINVAR
Blepharoptosis
CUI: C0005745
Disease: Blepharoptosis
0.700 GeneticVariation CLINVAR
Short neck
CUI: C0521525
Disease: Short neck
0.700 GeneticVariation CLINVAR
Intracranial Hemorrhage
CUI: C0151699
Disease: Intracranial Hemorrhage
0.700 GeneticVariation CLINVAR
BLADDER CANCER, TRANSITIONAL CELL, SOMATIC
0.700 CausalMutation CLINVAR