rs104894229, LRRC56;HRAS

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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.020 1.000 2 2012 2020
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.020 1.000 2 2012 2020
Alveolar rhabdomyosarcoma
CUI: C0206655
Disease: Alveolar rhabdomyosarcoma
1 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
Neoplasm, Residual
CUI: C0242596
Disease: Neoplasm, Residual
23 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
NEVUS, EPIDERMAL (disorder)
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
17 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.710 1.000 1 2019 2019
Costello syndrome (disorder)
CUI: C0587248
Disease: Costello syndrome (disorder)
24 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.900 1.000 31 2005 2018
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Noonan syndrome-like disorder with loose anagen hair
3 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 5 2007 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 3 2006 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.020 1.000 2 2016 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adenoid Cystic Carcinoma
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
30 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.564 0.600 11 534289 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 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016