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: rs2476601
rs2476601
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.860 0.900 3 2005 2018
dbSNP: rs2111485
rs2111485
0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2016
dbSNP: rs2395185
rs2395185
0.724 0.360 6 32465390 intron variant G/T snv 0.29
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs4409785
rs4409785
0.752 0.240 11 95578258 intron variant T/C snv 0.13
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012
dbSNP: rs12153855
rs12153855
0.776 0.320 6 32107027 intron variant T/C snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3132580
rs3132580
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3134942
rs3134942
0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.810 1.000 3 2010 2015
dbSNP: rs11203203
rs11203203
0.807 0.240 21 42416077 intron variant G/A snv 0.28
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 2 2010 2012
dbSNP: rs10484554
rs10484554
0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs13199524
rs13199524
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3131296
rs3131296
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs706779
rs706779
0.827 0.160 10 6056861 intron variant T/C snv 0.48
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.810 1.000 3 2010 2016
dbSNP: rs3806156
rs3806156
0.827 0.280 6 32405921 intron variant G/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 2 2010 2012
dbSNP: rs12198173
rs12198173
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3134945
rs3134945
0.827 0.240 6 32178715 intron variant C/A snv 0.18
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3757247
rs3757247
0.827 0.320 6 90247744 intron variant C/T snv 0.38
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012
dbSNP: rs1393350
rs1393350
0.851 0.160 11 89277878 intron variant G/A snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 3 2010 2012
dbSNP: rs1129038
rs1129038
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012
dbSNP: rs11966200
rs11966200
0.851 0.040 6 31869289 intron variant C/T snv 2.9E-02 4.5E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.810 0.500 1 2010 2013
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
dbSNP: rs2858870
rs2858870
0.851 0.280 6 32604474 intergenic variant T/A;C snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3130457
rs3130457
0.851 0.120 6 31179417 intron variant T/C snv 0.21
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs4766578
rs4766578
0.851 0.200 12 111466567 intron variant T/A snv 0.66
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012