rs367023, LINC00299

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.
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 1.000 0.040 2 8309993 intron variant A/G snv 0.35 0.800 1.000 2 2013 2016
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 1.000 0.040 2 8309993 intron variant A/G snv 0.35 0.700 1.000 1 2019 2019