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: rs4128561
rs4128561
1.000 0.080 11 128545234 intron variant T/C snv 0.58
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2016 2016
dbSNP: rs4937333
rs4937333
0.882 0.120 11 128460625 3 prime UTR variant T/C snv 0.45
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs4937334
rs4937334
11 128465683 intron variant G/A snv 0.22
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs6590334
rs6590334
1.000 0.040 11 128533313 intron variant T/C snv 0.60
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2015 2015
dbSNP: rs67232546
rs67232546
1.000 0.080 11 128529043 non coding transcript exon variant C/T snv 0.17
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2018 2018
dbSNP: rs7108992
rs7108992
11 128511972 intron variant A/C snv 0.71
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs7924522
rs7924522
1.000 0.040 11 128510847 intron variant C/A snv 0.70
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2018 2018
dbSNP: rs8705
rs8705
11 128459018 3 prime UTR variant G/A;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs8705
rs8705
11 128459018 3 prime UTR variant G/A;T snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs8705
rs8705
11 128459018 3 prime UTR variant G/A;T snv
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs8705
rs8705
11 128459018 3 prime UTR variant G/A;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016