rs925489, PTCSC2

N. diseases: 6
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.
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.800 1.000 2 2011 2012
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.800 1.000 2 2010 2018
Thyroid stimulating hormone measurement
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
83 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.800 1.000 1 2014 2014
Blood thyroid stimulating hormone analysis
CUI: C0696098
Disease: Blood thyroid stimulating hormone analysis
7 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.700 1.000 1 2014 2014
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.700 1.000 1 2012 2012
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.010 1.000 1 2014 2014