Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12990503
rs12990503
0.925 0.080 2 217429494 intron variant C/G snv 0.64
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.030 0.667 3 2013 2019