rs10180754, LINC01934

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 2 181238244 splice region variant G/A snv 0.35 0.700 1.000 1 2019 2019