rs7028661, PTCSC2

N. diseases: 4
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.
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.882 0.080 9 97776188 intron variant A/G snv 0.72 0.700 1.000 1 2012 2012
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.882 0.080 9 97776188 intron variant A/G snv 0.72 0.010 1.000 1 2015 2015
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.882 0.080 9 97776188 intron variant A/G snv 0.72 0.010 1.000 1 2015 2015
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.882 0.080 9 97776188 intron variant A/G snv 0.72 0.010 1.000 1 2015 2015