rs727503094, LRRC56;HRAS

N. diseases: 41
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 tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2006 2006
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2017 2017
melanoma
CUI: C0025202
Disease: melanoma
515 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2016 2016
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2017 2017
Neuromuscular Diseases
CUI: C0027868
Disease: Neuromuscular Diseases
50 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2017 2017
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2015 2015
Organoid Nevus Phakomatosis
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
9 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2019 2019
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2019 2019
Papilloma
CUI: C0030354
Disease: Papilloma
27 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
Pilocytic Astrocytoma
CUI: C0334583
Disease: Pilocytic Astrocytoma
14 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2007 2007
Precancerous Conditions
CUI: C0032927
Disease: Precancerous Conditions
18 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2015 2015
Seborrheic keratosis
CUI: C0022603
Disease: Seborrheic keratosis
21 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
Secondary malignant neoplasm of lymph node
188 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2015 2015
Thymic Carcinoma
CUI: C0205969
Disease: Thymic Carcinoma
8 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2009 2009
Thymoma
CUI: C0040100
Disease: Thymoma
20 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2009 2009
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2011 2011