rs2281388, HLA-DPA2

N. diseases: 4
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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.851 0.400 6 33092341 non coding transcript exon variant G/A snv 2.6E-02 0.800 1.000 2 2011 2019
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.851 0.400 6 33092341 non coding transcript exon variant G/A snv 2.6E-02 0.700 1.000 2 2009 2011
Thyrotoxic periodic paralysis
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
32 0.851 0.400 6 33092341 non coding transcript exon variant G/A snv 2.6E-02 0.700 1.000 1 2019 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.851 0.400 6 33092341 non coding transcript exon variant G/A snv 2.6E-02 0.020 1.000 2 2013 2015