rs10759944, 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.
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.925 0.080 9 97794690 intron variant A/G snv 0.72 0.710 1.000 3 2011 2014
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.925 0.080 9 97794690 intron variant A/G snv 0.72 0.700 1.000 3 2009 2013
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.925 0.080 9 97794690 intron variant A/G snv 0.72 0.700 1.000 1 2012 2012
Thyroid stimulating hormone measurement
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
83 0.925 0.080 9 97794690 intron variant A/G snv 0.72 0.700 1.000 1 2014 2014