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: 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: 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: 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: 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: 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: 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: 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: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2012 2016
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: 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: 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: 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: 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: 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: rs4409785
rs4409785 		0.752 0.240 11 95578258 intron variant T/C snv 0.13
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2012 2012
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: rs638893
rs638893 		0.882 0.080 11 118827828 intergenic variant G/A snv 0.79
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.820 1.000 1 2013 2017
dbSNP: rs736374
rs736374 		0.925 0.080 11 35245397 regulatory region variant G/A snv 0.29
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 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