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: 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: 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: 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
dbSNP: rs9501447
rs9501447 		1.000 0.040 6 30430063 intergenic variant A/G snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs3130284
rs3130284
AGPAT1
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: rs769449
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2012 2012
dbSNP: rs17195551
rs17195551
ATAT1
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: rs4766578
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2012 2012
dbSNP: rs3757247
rs3757247
BACH2
0.827 0.320 6 90247744 intron variant C/T snv 0.38
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2012 2012
dbSNP: rs3806156
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 2 2010 2012
dbSNP: rs28362683
rs28362683
BTNL2 ; TSBP1-AS1
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: rs229527
rs229527
C1QTNF6
0.925 0.160 22 37185445 missense variant C/A;G snv 0.43
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 3 2010 2016
dbSNP: rs3814231
rs3814231
CASP7
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: rs130065
rs130065
CCHCR1
0.925 0.120 6 31154723 missense variant G/A snv 0.15 0.16
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs16872571
rs16872571
CLNK
0.925 0.080 4 10725229 intergenic variant C/T snv 0.33
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2012 2012
dbSNP: rs11966200
rs11966200
CYP21A2 ; SLC44A4
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: rs7746003
rs7746003
DDR1-DT
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