Source: GWASCAT

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: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 2 2008 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: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.810 1.000 1 2010 2015
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: 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: rs13093110
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2012 2012
dbSNP: rs13093110
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.700 1.000 1 2012 2012
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: rs66756607
rs66756607
LPP
1.000 0.080 3 188365131 intron variant T/C snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
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: rs6444305
rs6444305
LPP
0.925 0.120 3 188582114 intron variant G/A;C;T snv
CUI: C1334633
Disease: Mature B-Cell Neoplasm
Mature B-Cell Neoplasm 		0.700 1.000 1 2014 2014
dbSNP: rs9864529
rs9864529
LPP
1.000 0.040 3 188387268 intron variant G/A snv 0.52
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		0.700 1.000 1 2015 2015
dbSNP: rs11715549
rs11715549
LPP
1.000 0.080 3 188370330 intron variant C/A;G snv
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin 		0.700 1.000 1 2016 2016
dbSNP: rs150062338
rs150062338
LPP
1.000 0.080 3 188287160 intron variant C/T snv 3.6E-02
CUI: C0243026
Disease: Sepsis
Sepsis 		0.700 1.000 1 2016 2016
dbSNP: rs191177147
rs191177147
LPP
0.882 0.040 3 188374758 intron variant G/T snv
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs191177147
rs191177147
LPP
0.882 0.040 3 188374758 intron variant G/T snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs191177147
rs191177147
LPP
0.882 0.040 3 188374758 intron variant G/T snv
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2016 2016
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2016 2016
dbSNP: rs542618547
rs542618547
LPP
3 188728876 intron variant AAA/-;A;AA;AAAA;AAAAA delins 0.23
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs542618547
rs542618547
LPP
3 188728876 intron variant AAA/-;A;AA;AAAA;AAAAA delins 0.23
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs6762714
rs6762714
LPP
1.000 0.080 3 188752450 intron variant C/T snv 0.53
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2016 2016
dbSNP: rs73196739
rs73196739
LPP
0.925 0.120 3 188684683 intron variant C/T snv 0.13
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2016 2016
dbSNP: rs9815073
rs9815073
LPP
0.925 0.120 3 188397894 intron variant C/A;G snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 1.000 1 2016 2016
dbSNP: rs9815073
rs9815073
LPP
0.925 0.120 3 188397894 intron variant C/A;G snv
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.700 1.000 1 2016 2016