HRAS, HRas proto-oncogene, GTPase, 3265

N. diseases: 698; N. variants: 29
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C4552097
Disease:
Nevus Sebaceus of Jadassohn
A 0.800 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C4552097
Disease:
Nevus Sebaceus of Jadassohn
G 0.800 CausalMutation CLINVAR
dbSNP: rs104894231
rs104894231
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0587248
Disease:
Costello syndrome (disorder)
T 0.800 CausalMutation CLINVAR
dbSNP: rs121917759
rs121917759
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0587248
Disease:
Costello syndrome (disorder)
A 0.800 CausalMutation CLINVAR
dbSNP: rs28933406
rs28933406
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C4225426
Disease:
THYROID CANCER, NONMEDULLARY, 2
T 0.800 CausalMutation CLINVAR
dbSNP: rs104894230
rs104894230
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0265329
Disease:
Organoid Nevus Phakomatosis
G 0.720 CausalMutation CLINVAR
dbSNP: rs121913233
rs121913233
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0025202
Disease:
melanoma
0.720 GeneticVariation UNIPROT
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0265329
Disease:
Organoid Nevus Phakomatosis
G 0.710 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0265329
Disease:
Organoid Nevus Phakomatosis
A 0.710 CausalMutation CLINVAR
dbSNP: rs104894229
rs104894229
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0334082
Disease:
NEVUS, EPIDERMAL (disorder)
A 0.710 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C4225657
Disease:
NEVUS SPILUS, SOMATIC
G 0.700 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0334082
Disease:
NEVUS, EPIDERMAL (disorder)
G 0.700 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C4551602
Disease:
Noonan Syndrome 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C1842036
Disease:
GIANT PIGMENTED HAIRY NEVUS
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C4225656
Disease:
SPITZ NEVUS, SOMATIC
G 0.700 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0334082
Disease:
NEVUS, EPIDERMAL (disorder)
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C4225426
Disease:
THYROID CANCER, NONMEDULLARY, 2
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894228
rs104894228
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0005684
Disease:
Malignant neoplasm of urinary bladder
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894229
rs104894229
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C4552097
Disease:
Nevus Sebaceus of Jadassohn
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894229
rs104894229
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C3854181
Disease:
Nevus sebaceous
T 0.700 CausalMutation CLINVAR
dbSNP: rs104894229
rs104894229
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0521525
Disease:
Short neck
T 0.700 CausalMutation CLINVAR
dbSNP: rs104894229
rs104894229
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C0005684
Disease:
Malignant neoplasm of urinary bladder
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894229
rs104894229
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C1968782
Disease:
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES
T 0.700 CausalMutation CLINVAR
dbSNP: rs104894229
rs104894229
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C3277679
Disease:
EPIDERMAL NEVUS WITH UROTHELIAL CANCER, SOMATIC
T 0.700 CausalMutation CLINVAR
dbSNP: rs104894229
rs104894229
Entrez Id: 3265;115399
Gene Symbol: HRAS;LRRC56
HRAS;LRRC56
CUI: C3854181
Disease:
Nevus sebaceous
A 0.700 CausalMutation CLINVAR