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: 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: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1.000 2 2008 2010
dbSNP: rs13067593
rs13067593
LPP
3 188866891 intron variant A/G snv 0.12
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement
0.800 1.000 1 2012 2012
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: rs13093110
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.800 1.000 1 2012 2012
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1.000 1 2011 2011
dbSNP: rs9851967
rs9851967
LPP
1.000 0.040 3 188369840 intron variant C/T snv 0.35
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2013 2013
dbSNP: rs9860547
rs9860547
LPP
0.925 0.080 3 188411191 intron variant G/A snv 0.34
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.800 1.000 1 2013 2013
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 2 2011 2011
dbSNP: rs1035765
rs1035765
LPP
3 188402995 intron variant A/T snv 0.38
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs1035766
rs1035766
LPP
3 188402952 intron variant G/A snv 0.38
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs11709294
rs11709294
LPP
3 188380247 intron variant T/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs11709472
rs11709472
LPP
3 188359798 intron variant C/T snv 0.35
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs11715716
rs11715716
LPP
3 188370852 intron variant C/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs12485444
rs12485444
LPP
3 188417995 intron variant T/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs12485704
rs12485704
LPP
3 188391978 intron variant C/T snv 0.42
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs12639588
rs12639588
LPP
3 188403475 intron variant A/G snv 0.34
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs13076312
rs13076312
LPP
1.000 0.040 3 188371466 intron variant C/T snv 0.44
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs13079741
rs13079741
LPP
3 188384073 intron variant G/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
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: rs13091753
rs13091753
LPP
1.000 0.040 3 188396801 intron variant G/C;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs13093110
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs13098877
rs13098877
LPP
3 188415375 intron variant C/T snv 0.41
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs13099273
rs13099273
LPP
1.000 0.080 3 188415730 intron variant A/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
0.700 1.000 1 2011 2011