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: rs1036332
rs1036332
1 199043349 intron variant A/C snv 0.70
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs11204682
rs11204682
1 150623061 intron variant G/A;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs114269697
rs114269697
1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs159963
rs159963
1.000 0.040 1 8444361 intron variant C/A snv 0.52
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs2075995
rs2075995
1 23520972 missense variant C/A snv 0.45 0.39
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs2296618
rs2296618
1 198697103 intron variant A/G snv 0.21
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs6684992
rs6684992
1 87286317 intergenic variant A/T snv 0.20
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2018
dbSNP: rs1004870
rs1004870
1 41905116 intron variant C/T snv 0.57
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1013910
rs1013910
1 116868761 intergenic variant G/A snv 0.91
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1071849
rs1071849
1 26320235 missense variant A/G snv 0.67 0.70
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs10794666
rs10794666
1 24924339 intron variant C/T snv 0.45
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs10864462
rs10864462
1 10552101 intron variant A/T snv 0.11
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1099448
rs1099448
1 173262759 intergenic variant C/T snv 0.58
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: 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: rs11264296
rs11264296
1 155022274 intron variant T/C snv 0.45
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
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: rs114695117
rs114695117
1 64743428 upstream gene variant C/A;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs11576941
rs11576941
1 46409395 intron variant G/T snv 0.27
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs11583398
rs11583398
1 206795610 intron variant C/A snv 9.9E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs11588625
rs11588625
HLX
1 220885504 downstream gene variant T/C snv 0.13
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1208984
rs1208984
1 11935119 intron variant A/G snv 0.42
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs12239046
rs12239046
1 247438293 intron variant T/C snv 0.58
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs12403425
rs12403425
1 197845693 intergenic variant C/A snv 0.17
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs12408934
rs12408934
1 64957764 intron variant G/A snv 6.1E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016