rs10489626, IL12RB2

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 1 67327488 intron variant C/G;T snv 0.17 0.700 1.000 1 2019 2019