Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs115429849
rs115429849
1.000 0.080 6 30416827 intron variant G/A snv
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic
Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9261858
rs9261858
1.000 0.040 6 30416540 non coding transcript exon variant G/A;C snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs9261862
rs9261862
1.000 0.040 6 30416961 intron variant C/G snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs9261871
rs9261871
1.000 0.040 6 30418117 intron variant A/G snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010