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: rs1468063
rs1468063
0.851 0.200 10 89015534 3 prime UTR variant C/T snv 0.17 0.17
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1571013
rs1571013
1.000 0.080 10 88998592 intron variant A/G snv 0.40
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1800682
rs1800682
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2015 2015