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: rs10810657
rs10810657
0.827 0.080 9 16884588 regulatory region variant T/A;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs10822220
rs10822220
10 63841301 intron variant A/G snv 0.17
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs10858740
rs10858740
12 88451258 intergenic variant A/G;T snv 0.56
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs10934582
rs10934582
3 122294507 downstream gene variant G/A snv 0.28
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs11077961
rs11077961
17 83054873 upstream gene variant A/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs11082513
rs11082513
18 46167187 intergenic variant C/T snv 0.42
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs111526888
rs111526888
18 60304392 downstream gene variant A/C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs11164971
rs11164971
1 91576688 regulatory region variant T/G snv 0.15
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs111678372
rs111678372
5 36087768 intergenic variant C/T snv 1.2E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs111759324
rs111759324
1 101186966 upstream gene variant C/T snv 0.11
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs11242709
rs11242709
1.000 0.040 6 209159 upstream gene variant C/T snv 0.19
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs11265402
rs11265402
1 160443300 regulatory region variant C/T snv 0.18
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs112711080
rs112711080
2 37335250 upstream gene variant C/T snv 5.2E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs113252371
rs113252371
16 30465196 intergenic variant C/T snv 0.15
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs113317835
rs113317835
7 3088056 intron variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs11359909
rs11359909
3 128603031 intergenic variant G/- delins 0.89
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs113844630
rs113844630
12 116899298 intergenic variant T/C snv 0.21
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs114050631
rs114050631
2 218156235 regulatory region variant C/T snv 6.9E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs114422334
rs114422334
6 31263867 downstream gene variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2018 2018
dbSNP: rs114965247
rs114965247
6 31382526 upstream gene variant T/A;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2018 2018
dbSNP: rs115039395
rs115039395
2 102545057 intergenic variant C/G snv 1.4E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs115978073
rs115978073
2 213186248 intergenic variant T/C snv 5.1E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs11603634
rs11603634
1.000 0.080 11 1142570 intergenic variant A/G snv 0.38
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs11658674
rs11658674
17 78245707 upstream gene variant T/C snv 0.20
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs116847786
rs116847786
22 28765016 intergenic variant G/A snv 4.6E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019