rs7848973, PTCSC2

N. diseases: 2
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 97826557 intron variant A/G snv 0.67 0.700 1.000 1 2012 2012
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.925 0.080 9 97826557 intron variant A/G snv 0.67 0.700 1.000 1 2013 2013