Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894231
rs104894231
HRAS ; LRRC56
T 0.800 CausalMutation CLINVAR

dbSNP: rs121917759
rs121917759
HRAS ; LRRC56
A 0.800 CausalMutation CLINVAR

dbSNP: rs35613389
rs35613389
HRAS ; LRRC56
CG 0.700 CausalMutation CLINVAR

dbSNP: rs398122808
rs398122808
HRAS ; LRRC56
ACCT 0.700 CausalMutation CLINVAR

dbSNP: rs398122809
rs398122809
HRAS ; LRRC56
CTCT 0.700 CausalMutation CLINVAR

dbSNP: rs587777239
rs587777239
HRAS ; LRRC56
GGTCCCGCATGGCGCTGTACTC 0.700 CausalMutation CLINVAR

dbSNP: rs727504747
rs727504747
HRAS ; LRRC56
AG 0.700 GeneticVariation CLINVAR

dbSNP: rs104894230
rs104894230
HRAS ; LRRC56
T 0.840 CausalMutation CLINVAR Carcinogen-induced mutations in the mouse c-Ha-ras gene provide evidence of multiple pathways for tumor progression. 2105486

1990
dbSNP: rs727503093
rs727503093
HRAS ; LRRC56
T 0.700 GeneticVariation CLINVAR rac, a novel ras-related family of proteins that are botulinum toxin substrates. 2674130

1989
dbSNP: rs727503093
rs727503093
HRAS ; LRRC56
T 0.700 GeneticVariation CLINVAR Ras p21 proteins with high or low GTPase activity can efficiently transform NIH/3T3 cells. 3004741

1986
dbSNP: rs727503093
rs727503093
HRAS ; LRRC56
T 0.700 GeneticVariation CLINVAR The ras gene family and human carcinogenesis. 3283542

1988
dbSNP: rs727503093
rs727503093
HRAS ; LRRC56
T 0.700 GeneticVariation CLINVAR ras genes. 3304147

1987
dbSNP: rs727503093
rs727503093
HRAS ; LRRC56
T 0.700 GeneticVariation CLINVAR Nucleotide sequence of the p21 transforming protein of Harvey murine sarcoma virus. 6287572

1982
dbSNP: rs727503093
rs727503093
HRAS ; LRRC56
T 0.700 GeneticVariation CLINVAR Nucleotide sequence of the oncogene encoding the p21 transforming protein of Kirsten murine sarcoma virus. 6287573

1982
dbSNP: rs727503093
rs727503093
HRAS ; LRRC56
T 0.700 GeneticVariation CLINVAR Characterization of the phosphorylation sites and the surrounding amino acid sequences of the p21 transforming proteins coded for by the Harvey and Kirsten strains of murine sarcoma viruses. 6288698

1982
dbSNP: rs727503093
rs727503093
HRAS ; LRRC56
T 0.700 GeneticVariation CLINVAR Role of the switch II region in the conformational transition of activation of Ha-ras-p21. 10716188

2000
dbSNP: rs104894229
rs104894229
HRAS ; LRRC56
0.900 GeneticVariation UNIPROT Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005
dbSNP: rs104894229
rs104894229
HRAS ; LRRC56
T 0.900 CausalMutation CLINVAR Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005
dbSNP: rs104894230
rs104894230
HRAS ; LRRC56
A 0.840 CausalMutation CLINVAR Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005
dbSNP: rs104894230
rs104894230
HRAS ; LRRC56
G 0.840 CausalMutation CLINVAR Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005
dbSNP: rs104894230
rs104894230
HRAS ; LRRC56
0.840 GeneticVariation UNIPROT Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005
dbSNP: rs104894228
rs104894228
HRAS ; LRRC56
0.830 GeneticVariation UNIPROT Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005
dbSNP: rs104894226
rs104894226
HRAS ; LRRC56
T 0.810 CausalMutation CLINVAR Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005
dbSNP: rs104894226
rs104894226
HRAS ; LRRC56
0.810 GeneticVariation UNIPROT Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005
dbSNP: rs104894227
rs104894227
HRAS ; LRRC56
0.810 GeneticVariation UNIPROT Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005