rs10983700, 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.
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 1.000 0.080 9 97775173 intron variant T/A;C snv 0.700 1.000 1 2012 2012
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 1.000 0.080 9 97775173 intron variant T/A;C snv 0.700 1.000 1 2010 2010