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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.710 1.000 2 2014 2014
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2018 2018
Eccrine porocarcinoma
CUI: C1266065
Disease: Eccrine porocarcinoma
11 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2018 2018
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2014 2014
Follicular Variant Thyroid Gland Papillary Carcinoma
CUI: C3714651
Disease: Follicular Variant Thyroid Gland Papillary Carcinoma
13 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2013 2013
Inverted urothelial papilloma
CUI: C1334282
Disease: Inverted urothelial papilloma
3 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2014 2014
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2014 2014
melanoma
CUI: C0025202
Disease: melanoma
515 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2018 2018
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2019 2019
Recurrent tumor
CUI: C0521158
Disease: Recurrent tumor
33 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2016 2016
Solid/Multicystic Ameloblastoma
CUI: C1513734
Disease: Solid/Multicystic Ameloblastoma
10 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 0.010 1.000 1 2019 2019