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: rs3213758
rs3213758
RPGRIP1L
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: 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: rs9468925
rs9468925
HLA-B
0.851 0.040 6 31291060 intron variant G/A snv 0.44
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.820 1.000 1 2010 2012
dbSNP: rs10876864
rs10876864
IKZF4
0.882 0.120 12 56007301 upstream gene variant G/A snv 0.50
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.810 1.000 1 2013 2013
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: rs13208776
rs13208776
SMOC2
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: rs1417210
rs1417210
SLC29A3
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: rs2456973
rs2456973
IKZF4 ; LOC105369780 ; LOC105369781
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: 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: rs7758128
rs7758128
TSBP1-AS1
0.882 0.040 6 32377506 intron variant C/A;T snv 4.2E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.810 1.000 1 2011 2011
dbSNP: rs10768122
rs10768122
SLC1A2
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: 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: rs1129038
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2012 2012
dbSNP: rs11593576
rs11593576
ZMIZ1
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: 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: 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: 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: rs2236313
rs2236313
RNASET2
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: 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: 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: rs3823355
rs3823355
HLA-A ; HCG9
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
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: 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: 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: rs6510827
rs6510827
TICAM1
1.000 0.040 19 4830616 intron variant T/C snv 0.66
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2012 2012