rs121913233, HRAS;LRRC56

N. diseases: 37
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.
Nevus Sebaceus of Jadassohn
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
7 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 0
Organoid Nevus Phakomatosis
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
9 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 0
Skin Carcinogenesis
CUI: C1519346
Disease: Skin Carcinogenesis
7 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2012 2012
Follicular Variant Thyroid Gland Papillary Carcinoma
CUI: C3714651
Disease: Follicular Variant Thyroid Gland Papillary Carcinoma
13 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2013 2013
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Inverted urothelial papilloma
CUI: C1334282
Disease: Inverted urothelial papilloma
3 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Papilloma
CUI: C0030354
Disease: Papilloma
27 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Trichilemmoma
CUI: C0334263
Disease: Trichilemmoma
4 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 5 2007 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
92 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 4 2012 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Adrenal Gland Pheochromocytoma
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
50 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Paraganglioma
CUI: C0030421
Disease: Paraganglioma
36 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016