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: 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: 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: rs229527
rs229527
0.925 0.160 22 37185445 missense variant C/A;G snv 0.43
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 3 2010 2016
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: 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: 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: rs4908760
rs4908760
1.000 0.040 1 8466082 intron variant G/A snv 0.68
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 2 2010 2012
dbSNP: rs532098
rs532098
0.882 0.120 6 32610275 intergenic variant G/A snv 0.43
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 2 2010 2012
dbSNP: rs6902119
rs6902119
0.882 0.160 6 167092303 intron variant T/C;G snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 2 2010 2012
dbSNP: rs8192917
rs8192917
0.925 0.040 14 24632954 missense variant C/T snv 0.76 0.72
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.810 1.000 2 2010 2018
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: rs1079541
rs1079541
1.000 0.040 6 30438979 intergenic variant C/A snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs11593576
rs11593576
0.925 0.040 10 79256139 intron variant C/T snv 0.29
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2010 2010
dbSNP: rs11964542
rs11964542
1.000 0.040 6 30103983 non coding transcript exon variant T/C snv 7.2E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: rs11966619
rs11966619
1.000 0.040 6 30461256 intergenic variant T/G snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs11967808
rs11967808
1.000 0.040 6 30211411 intron variant G/C snv 3.2E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: 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: rs12201301
rs12201301
1.000 0.040 6 31039780 downstream gene variant G/A snv 2.7E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs12206131
rs12206131
1.000 0.040 6 31446233 non coding transcript exon variant A/G snv 1.8E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs1264350
rs1264350
0.925 0.160 6 30828768 intron variant T/C snv 9.4E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs1264377
rs1264377
1.000 0.040 6 30797130 downstream gene variant G/A snv 0.13
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs1265159
rs1265159
0.882 0.240 6 31172270 intron variant G/A snv 0.21
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010