rs7850258, PTCSC2

N. diseases: 3
Source: CURATED ×
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
245 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.820 1.000 3 2011 2019
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
41 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.710 1.000 2 2010 2015
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.700 1.000 1 2012 2012