rs17606253, SLC16A10

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.
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 1.000 0.040 6 111205242 intron variant T/C snv 0.12 0.010 1.000 1 2017 2017