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: 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: 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: 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: 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: 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: rs3132649
rs3132649
1.000 0.040 6 30353280 downstream gene variant G/A snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs3213758
rs3213758
0.925 0.040 16 53605526 missense variant C/T snv 7.3E-02 4.7E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.820 1.000 1 2013 2015
dbSNP: rs3218822
rs3218822
1.000 0.040 6 30912559 intron variant T/C snv 1.9E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs33986393
rs33986393
1.000 0.040 6 30456297 downstream gene variant A/G snv 0.16
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: rs34214527
rs34214527
0.925 0.040 6 32046679 intron variant C/T snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs35407515
rs35407515
1.000 0.040 6 30455446 non coding transcript exon variant A/G snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
dbSNP: rs35792611
rs35792611
1.000 0.040 6 30463098 upstream gene variant C/G snv 0.16
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2010 2010
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