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.
Acute monoblastic leukemia
CUI: C0457334
Disease: Acute monoblastic leukemia
5 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
Adult Acute Monoblastic Leukemia
CUI: C0279629
Disease: Adult Acute Monoblastic Leukemia
5 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
Childhood Acute Monoblastic Leukemia
CUI: C0279645
Disease: Childhood Acute Monoblastic Leukemia
5 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
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
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
Adult Pilocytic Astrocytoma
CUI: C0280781
Disease: Adult Pilocytic Astrocytoma
10 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2007 2007
Childhood Pilocytic Astrocytoma
CUI: C1332995
Disease: Childhood Pilocytic Astrocytoma
10 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2007 2007
Ductal Carcinoma
CUI: C1176475
Disease: Ductal Carcinoma
11 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2016 2016
Juberg-Marsidi syndrome
CUI: C0796003
Disease: Juberg-Marsidi syndrome
14 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2019 2019
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
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
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
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
22 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
Costello syndrome (disorder)
CUI: C0587248
Disease: Costello syndrome (disorder)
24 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.750 1.000 6 2006 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
Arthrogryposis
CUI: C0003886
Disease: Arthrogryposis
33 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2017 2017
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
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 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
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
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
leukemia
CUI: C0023418
Disease: leukemia
144 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
CUI: C0686619
Disease: 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
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.020 1.000 2 2015 2017