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: rs3213758
rs3213758
0.925 0.040 16 53605526 missense variant C/T snv 7.3E-02 4.7E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.820 1.000 1 2013 2015
dbSNP: rs638893
rs638893
0.882 0.080 11 118827828 intergenic variant G/A snv 0.79
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.820 1.000 1 2013 2017
dbSNP: rs9468925
rs9468925
0.851 0.040 6 31291060 intron variant G/A snv 0.44
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.820 1.000 1 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: 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: 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: 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: 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: rs13208776
rs13208776
0.882 0.040 6 168540944 intron variant G/A;C snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.810 0.500 1 2010 2011
dbSNP: rs1417210
rs1417210
0.925 0.040 10 71376162 intron variant G/A;C snv
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: rs59374417
rs59374417
0.925 0.040 3 119569567 intergenic variant A/C;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.810 1.000 1 2012 2015
dbSNP: rs7758128
rs7758128
0.882 0.040 6 32377506 intron variant C/A;T snv 4.2E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.810 1.000 1 2011 2011
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: 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: 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: rs10768122
rs10768122
1.000 0.040 11 35259305 3 prime UTR variant A/G snv 0.33
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012
dbSNP: rs11021232
rs11021232
1.000 0.040 11 95587644 intron variant T/C snv 0.14
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2016
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: 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: rs13076312
rs13076312
LPP
1.000 0.040 3 188371466 intron variant C/T snv 0.44
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2010 2016
dbSNP: rs16872571
rs16872571
0.925 0.080 4 10725229 intergenic variant C/T snv 0.33
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012