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: 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: 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: 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: rs13091753
rs13091753
LPP
1.000 0.040 3 188396801 intron variant G/C;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs13118
rs13118
1.000 0.040 6 31859509 3 prime UTR variant A/G;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: rs1548514
rs1548514
1.000 0.040 6 30419691 downstream gene variant G/A;C;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs17190134
rs17190134
1.000 0.040 6 31054083 non coding transcript exon variant C/A;G snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs2248902
rs2248902
1.000 0.040 6 31266337 downstream gene variant G/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: rs28383344
rs28383344
1.000 0.040 6 32637290 intron variant C/G;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs2839511
rs2839511
1.000 0.040 21 42428412 intron variant G/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2011 2011
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: rs301819
rs301819
0.882 0.120 1 8441726 intron variant A/G;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2011 2011
dbSNP: rs3094061
rs3094061
0.925 0.160 6 30353412 downstream gene variant A/C;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3130424
rs3130424
0.925 0.040 6 31250462 intergenic variant A/C;G;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3130455
rs3130455
1.000 0.040 6 31158201 5 prime UTR variant A/C;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs34101875
rs34101875
1.000 0.040 6 30455581 non coding transcript exon variant G/A;C;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: 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: 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: rs9261858
rs9261858
1.000 0.040 6 30416540 non coding transcript exon variant G/A;C snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs17188127
rs17188127
1.000 0.040 6 30167325 intron variant C/T snv 9.9E-03
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010