Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879255268
rs879255268
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C4310789
Disease:
THROMBOCYTOPENIA 6
0.800 GeneticVariation UNIPROT A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies. 26936507 2016
dbSNP: rs879255268
rs879255268
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C4310789
Disease:
THROMBOCYTOPENIA 6
A 0.800 CausalMutation CLINVAR
dbSNP: rs879255268
rs879255268
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0040034
Disease:
Thrombocytopenia
0.710 GeneticVariation BEFREE We now report a 5-year-old girl with syndromic thrombocytopenia due to the same SRC-E527K variant that occurs <i>de novo</i>. 31204551 2019
dbSNP: rs879255268
rs879255268
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0040034
Disease:
Thrombocytopenia
A 0.710 GeneticVariation CLINVAR
dbSNP: rs754626
rs754626
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0007137
Disease:
Squamous cell carcinoma
G 0.700 GeneticVariation GWASCAT A Genome-Wide Association Study of Cutaneous Squamous Cell Carcinoma among European Descendants. 26908436 2016
dbSNP: rs121913314
rs121913314
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0027651
Disease:
Neoplasms
T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968 2014
dbSNP: rs121913314
rs121913314
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C4016406
Disease:
COLON CANCER, ADVANCED, SOMATIC
T 0.700 CausalMutation CLINVAR
dbSNP: rs879255268
rs879255268
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0001815
Disease:
Primary Myelofibrosis
A 0.700 GeneticVariation CLINVAR
dbSNP: rs768889863
rs768889863
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Significantly, ectopic expression of SUMO-defective mutation, Src K318R, promotes tumor growth more potently than that of wild-type Src, as determined by migration assay, soft agar assay, and tumor xenograft experiments. 29069627 2017
dbSNP: rs754626
rs754626
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0553723
Disease:
Squamous cell carcinoma of skin
0.010 GeneticVariation BEFREE Besides, we validated four other SNPs associated with SCC in the replication set, including rs9689649 in PARK2 gene (P = 2.7 × 10(-6) in combined set; P = 3.2 × 10(-5) in the discovery; and P = 0.02 in the replication), rs754626 in the SRC gene (P = 1.1 × 10(-6) in combined set; P = 1.4 × 10(-5) in the discovery and P = 0.02 in the replication), rs9643297 in ST3GAL1 gene (P = 8.2 × 10(-6) in combined set; P = 3.3 × 10(-5) in the discovery; and P = 0.04 in the replication), and rs17247181 in ERBB2IP gene (P = 4.2 × 10(-6) in combined set; P = 3.1 × 10(-5) in the discovery; and P = 0.048 in the replication). 26908436 2016
dbSNP: rs764262104
rs764262104
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C3887645
Disease:
Job Syndrome
0.010 GeneticVariation BEFREE These data suggest, that dominant negative mutations of the DNA-binding and SH2 domains of STAT3 cause AD and sporadic cases of HIES in different ethnic groups with R382W as the predominant mutation found in 5 of the 9 families. 18706697 2008
dbSNP: rs121913314
rs121913314
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0007102
Disease:
Malignant tumor of colon
0.010 GeneticVariation BEFREE A recent report suggested that the risk of colon cancer is higher for those who carry a C-->T transition mutation on codon 531 (Gln-531-->Amber-531) of src gene. 10704743 2000
dbSNP: rs121913314
rs121913314
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0476089
Disease:
Endometrial Carcinoma
0.010 GeneticVariation BEFREE We found one truncated mutation at codon 531 (Gln to Stop) in an endometrial carcinoma. 10804287 2000
dbSNP: rs121913314
rs121913314
Entrez Id: 6714
Gene Symbol: SRC
SRC
CUI: C0699790
Disease:
Colon Carcinoma
0.010 GeneticVariation BEFREE A recent report suggested that the risk of colon cancer is higher for those who carry a C-->T transition mutation on codon 531 (Gln-531-->Amber-531) of src gene. 10704743 2000