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
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
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
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
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
135 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 5 2007 2016
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
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 3 2014 2017
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.020 1.000 2 2015 2017
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
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 2 2014 2016
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
melanoma
CUI: C0025202
Disease: melanoma
515 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 2 2014 2016
Organoid Nevus Phakomatosis
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
9 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.720 1.000 2 2012 2019
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
Acute monoblastic leukemia
CUI: C0457334
Disease: Acute monoblastic leukemia
5 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
22 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014