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: rs1701704
rs1701704
0.851 0.200 12 56018703 intron variant T/G snv 0.25
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2012 2012
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
dbSNP: rs17188268
rs17188268
1.000 0.040 6 30231581 downstream gene variant G/A snv 3.2E-02
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: rs17195551
rs17195551
1.000 0.040 6 30633618 intron variant C/T snv 3.2E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs1847134
rs1847134
0.925 0.080 11 89272085 intron variant A/C snv 0.26
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: rs2395185
rs2395185
0.724 0.360 6 32465390 intron variant G/T snv 0.29
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs2523505
rs2523505
1.000 0.040 6 31542225 5 prime UTR variant C/G snv 7.6E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs2524123
rs2524123
0.925 0.040 6 31297537 intron variant T/C snv 0.34
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs28362683
rs28362683
1.000 0.040 6 32405186 synonymous variant G/A snv 0.12 0.10
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2011 2011
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: rs3096697
rs3096697
0.882 0.200 6 32166733 missense variant G/A snv 0.16 0.18
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3130284
rs3130284
0.925 0.120 6 32172710 intron variant T/C snv 0.18
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3130347
rs3130347
1.000 0.040 6 32166879 intron variant T/C snv 0.15 0.18
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: rs3130457
rs3130457
0.851 0.120 6 31179417 intron variant T/C snv 0.21
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3130473
rs3130473
0.882 0.160 6 31231431 intergenic variant C/T snv 0.23
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3131296
rs3131296
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010