rs17477923, FAM227B

N. diseases: 1
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.
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
27 1.000 0.040 15 49418988 intron variant T/C snv 0.22 0.700 1.000 1 2018 2018