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: 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
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: rs2236313
rs2236313
1.000 0.040 6 166946901 intron variant T/C snv 0.53 0.50
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 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: rs3814231
rs3814231
1.000 0.040 10 113721259 intron variant C/T snv 0.23
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012
dbSNP: rs3823355
rs3823355
1.000 0.040 6 29974306 upstream gene variant C/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 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: 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
dbSNP: rs4822024
rs4822024
1.000 0.040 22 41361643 downstream gene variant G/A;C snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012
dbSNP: rs6510827
rs6510827
1.000 0.040 19 4830616 intron variant T/C snv 0.66
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012
dbSNP: rs853308
rs853308
TG
1.000 0.040 8 132917672 intron variant C/T snv 0.41
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012
dbSNP: rs9851967
rs9851967
LPP
1.000 0.040 3 188369840 intron variant C/T snv 0.35
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2013 2013
dbSNP: rs9926296
rs9926296
1.000 0.040 16 89751681 intron variant A/G snv 0.54
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 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: 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: 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: 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