rs1188536960, SORD

N. diseases: 5
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.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.882 0.120 15 45043305 missense variant A/G snv 0.010 1.000 1 2015 2015
Follicular thyroid carcinoma
CUI: C0206682
Disease: Follicular thyroid carcinoma
28 0.882 0.120 15 45043305 missense variant A/G snv 0.010 1.000 1 2015 2015
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.882 0.120 15 45043305 missense variant A/G snv 0.010 1.000 1 2015 2015
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.882 0.120 15 45043305 missense variant A/G snv 0.010 1.000 1 2005 2005
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.882 0.120 15 45043305 missense variant A/G snv 0.010 1.000 1 2015 2015