rs104894230, HRAS;LRRC56

N. diseases: 73
Source: ALL
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.
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
COSTELLO SYNDROME, SEVERE
CUI: C4016398
Disease: COSTELLO SYNDROME, SEVERE
1 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
GIANT PIGMENTED HAIRY NEVUS
CUI: C1842036
Disease: GIANT PIGMENTED HAIRY NEVUS
6 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES
CUI: C1968782
Disease: MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES
4 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
Nevus sebaceous
CUI: C3854181
Disease: Nevus sebaceous
4 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
Nevus Sebaceus of Jadassohn
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
7 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
NEVUS, EPIDERMAL (disorder)
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
17 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
THYROID CANCER, NONMEDULLARY, 2
CUI: C4225426
Disease: THYROID CANCER, NONMEDULLARY, 2
13 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
Costello syndrome (disorder)
CUI: C0587248
Disease: Costello syndrome (disorder)
24 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.840 1.000 23 1990 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1 1999 1999
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.020 1.000 2 2006 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.020 1.000 2 2006 2015
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 5 2007 2016
Adult Pilocytic Astrocytoma
CUI: C0280781
Disease: Adult Pilocytic Astrocytoma
10 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Childhood Pilocytic Astrocytoma
CUI: C1332995
Disease: Childhood Pilocytic Astrocytoma
10 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Pilocytic Astrocytoma
CUI: C0334583
Disease: Pilocytic Astrocytoma
14 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Thymic Carcinoma
CUI: C0205969
Disease: Thymic Carcinoma
8 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Thymoma
CUI: C0040100
Disease: Thymoma
20 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.100 1.000 13 2010 2019
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.040 1.000 4 2011 2015
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 2 2011 2016