rs7850258, 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 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.820 1.000 4 2011 2019
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.710 1.000 3 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
Cleft palate with cleft lip
CUI: C0158646
Disease: Cleft palate with cleft lip
43 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.010 1.000 1 2015 2015
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.010 1.000 1 2015 2015
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.010 1.000 1 2015 2015