rs104894230, HRAS;LRRC56

N. diseases: 36
Source: CLINVAR ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Costello syndrome (disorder)
CUI: C0587248
Disease: Costello syndrome (disorder)
16 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.840 1.000 14 1990 2019
Organoid Nevus Phakomatosis
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
7 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.720 1.000 0 2012 2019
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
314 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 2 2014 2017
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
102 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 1 2011 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
141 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 1 2014 2016
melanoma
CUI: C0025202
Disease: melanoma
129 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 1 2014 2016
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
350 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 10 2002 2017
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
25 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 5 2007 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
211 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
114 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adenoid Cystic Carcinoma
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
27 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
216 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
153 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
188 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
115 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
142 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
76 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
19 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
17 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Papillary renal cell carcinoma, sporadic
CUI: C1336078
Disease: Papillary renal cell carcinoma, sporadic
30 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Serous cystadenocarcinoma ovary
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
99 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
54 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
179 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016