Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1701704
rs1701704
0.851 0.200 12 56018703 intron variant T/G snv 0.25
Diabetes Mellitus, Insulin-Dependent
0.830 1.000 1 2008 2013
dbSNP: rs10876864
rs10876864
0.882 0.120 12 56007301 upstream gene variant G/A snv 0.50
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.810 1.000 1 2013 2013
dbSNP: rs2456973
rs2456973
0.925 0.040 12 56023144 intron variant A/C;G snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.810 1.000 1 2012 2015
dbSNP: rs1701704
rs1701704
0.851 0.200 12 56018703 intron variant T/G snv 0.25
CUI: C0004096
Disease: Asthma
Asthma
0.800 1.000 1 2011 2011
dbSNP: rs1701704
rs1701704
0.851 0.200 12 56018703 intron variant T/G snv 0.25
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
0.800 1.000 1 2010 2010
dbSNP: rs1701704
rs1701704
0.851 0.200 12 56018703 intron variant T/G snv 0.25
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2011 2011
dbSNP: rs1701704
rs1701704
0.851 0.200 12 56018703 intron variant T/G snv 0.25
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2012 2012