rs104894228, LRRC56;HRAS

N. diseases: 48
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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.605 0.560 11 534286 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 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.605 0.560 11 534286 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
92 0.605 0.560 11 534286 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
348 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Costello syndrome (disorder)
CUI: C0587248
Disease: Costello syndrome (disorder)
24 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.830 1.000 16 2005 2017
Benign melanocytic nevus
CUI: C1456781
Disease: Benign melanocytic nevus
20 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Melanocytic nevus
CUI: C0027962
Disease: Melanocytic nevus
33 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Nevus
CUI: C0027960
Disease: Nevus
43 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Noonan syndrome-like disorder with loose anagen hair
CUI: C1843181
Disease: Noonan syndrome-like disorder with loose anagen hair
3 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Retinal Dystrophies
CUI: C0854723
Disease: Retinal Dystrophies
227 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Trichoepithelioma
CUI: C0349658
Disease: Trichoepithelioma
3 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 3 2006 2018
Adult Rhabdomyosarcoma
CUI: C0279550
Disease: Adult Rhabdomyosarcoma
12 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Childhood Rhabdomyosarcoma
CUI: C0220611
Disease: Childhood Rhabdomyosarcoma
12 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Eccrine porocarcinoma
CUI: C1266065
Disease: Eccrine porocarcinoma
11 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Rhabdomyosarcoma
CUI: C0035412
Disease: Rhabdomyosarcoma
20 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018