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: 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: 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: rs7746003
rs7746003
1.000 0.040 6 30875117 non coding transcript exon variant T/A snv 3.1E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: rs7759803
rs7759803
1.000 0.040 6 30844742 intron variant G/A snv 5.9E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: rs9261761
rs9261761
1.000 0.040 6 30405210 intergenic variant G/A snv 0.16
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9261817
rs9261817
1.000 0.040 6 30410824 upstream gene variant A/C snv 0.16
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9261821
rs9261821
1.000 0.040 6 30411297 upstream gene variant T/C snv 0.16
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9261846
rs9261846
1.000 0.040 6 30414663 upstream gene variant G/C snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: rs9261862
rs9261862
1.000 0.040 6 30416961 intron variant C/G snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9261871
rs9261871
1.000 0.040 6 30418117 intron variant A/G snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9261919
rs9261919
1.000 0.040 6 30423946 downstream gene variant G/A snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9261923
rs9261923
1.000 0.040 6 30424383 intergenic variant G/A snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9261926
rs9261926
1.000 0.040 6 30424629 intergenic variant C/A;T snv 0.19
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9261947
rs9261947
1.000 0.040 6 30426851 intergenic variant C/T snv 0.16
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9295822
rs9295822
1.000 0.040 6 29861103 intron variant C/T snv 0.12
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9295871
rs9295871
1.000 0.040 6 30443312 intergenic variant T/C snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9295873
rs9295873
1.000 0.040 6 30446458 upstream gene variant A/G snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9295886
rs9295886
1.000 0.040 6 30453620 intron variant C/T snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs9461612
rs9461612
1.000 0.040 6 30470779 downstream gene variant G/A snv 0.16
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: rs9501336
rs9501336
1.000 0.040 6 30459733 downstream gene variant G/A snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010