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.
Adult Fibrosarcoma
CUI: C0278595
Disease: Adult Fibrosarcoma
9 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Adult Rhabdomyosarcoma
CUI: C0279550
Disease: Adult Rhabdomyosarcoma
12 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
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
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
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
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
82 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Childhood Rhabdomyosarcoma
CUI: C0220611
Disease: Childhood Rhabdomyosarcoma
12 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Cutis Laxa
CUI: C0010495
Disease: Cutis Laxa
21 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2010 2010
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Fibrosarcoma
CUI: C0016057
Disease: Fibrosarcoma
9 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
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
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
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Noonan syndrome-like disorder with loose anagen hair
CUI: C1843181
Disease: 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
Respiratory distress
CUI: C0476273
Disease: Respiratory distress
16 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Rhabdomyosarcoma
CUI: C0035412
Disease: Rhabdomyosarcoma
20 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Thyroid Nodule
CUI: C0040137
Disease: Thyroid Nodule
17 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
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
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
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
Coarse facial features
CUI: C1845847
Disease: Coarse facial features
33 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 9 2005 2009
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 9 2005 2009
Deep palmar crease
CUI: C1857539
Disease: Deep palmar crease
8 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 9 2005 2009
Hydrocephalus
CUI: C0020255
Disease: Hydrocephalus
37 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 9 2005 2009