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: rs1393350
rs1393350
TYR ; LOC107984363
0.851 0.160 11 89277878 intron variant G/A snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 3 2010 2012
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.810 1.000 3 2010 2015
dbSNP: rs706779
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.810 1.000 3 2010 2016
dbSNP: rs11203203
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 2 2010 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: rs4908760
rs4908760
RERE
1.000 0.040 1 8466082 intron variant G/A snv 0.68
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 2 2010 2012
dbSNP: rs6902119
rs6902119
FGFR1OP
0.882 0.160 6 167092303 intron variant T/C;G snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 2 2010 2012
dbSNP: rs10484554
rs10484554
HLA-B ; LOC112267902
0.807 0.200 6 31306778 intron variant C/T snv 0.12
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: 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: 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: rs11967808
rs11967808
TRIM26
1.000 0.040 6 30211411 intron variant G/C snv 3.2E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs12153855
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs12198173
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs1264350
rs1264350
LINC00243
0.925 0.160 6 30828768 intron variant T/C snv 9.4E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs1265159
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 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: rs13091753
rs13091753
LPP
1.000 0.040 3 188396801 intron variant G/C;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs13199524
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
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: rs1559810
rs1559810
LPP
1.000 0.040 3 188406566 intron variant C/A snv 0.36
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs17008723
rs17008723
FOXP1
0.925 0.040 3 71523984 intron variant T/G snv 0.15
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2012 2012
dbSNP: rs1701704
rs1701704
IKZF4 ; LOC105369781
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
TRIM15
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