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: rs12206499
rs12206499
1.000 0.040 6 29969350 downstream gene variant A/G snv 0.27
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 2 2011 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: 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: 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: 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: 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: 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: 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: 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: rs1265181
rs1265181
0.925 0.040 6 31188008 intergenic variant G/C snv 0.15
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 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: 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: rs13204672
rs13204672
1.000 0.040 6 32615019 intergenic variant A/G snv 0.12
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: rs13211318
rs13211318
0.925 0.040 6 32134903 upstream gene variant A/C snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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: rs1559810
rs1559810
LPP
1.000 0.040 3 188406566 intron variant C/A snv 0.36
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs17008723
rs17008723
0.925 0.040 3 71523984 intron variant T/G snv 0.15
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2012 2012