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: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs140945396
rs140945396
7 49950222 intron variant G/A snv 7.7E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs74249949
rs74249949
16 30580789 3 prime UTR variant A/G snv 0.14
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs9889262
rs9889262
17 49320708 intron variant T/A snv 0.28
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs55972630
rs55972630
19 11802341 intron variant T/C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs703530
rs703530
19 37010016 intron variant G/A snv 0.35
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs4727027
rs4727027
7 149172185 intron variant G/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs6961605
rs6961605
7 149173016 intron variant G/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs16917546
rs16917546
0.851 0.040 10 62637778 intron variant T/C snv 0.29
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2018 2019
dbSNP: rs10995240
rs10995240
10 62628871 intron variant G/C snv 0.29
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs12413946
rs12413946
10 62671446 non coding transcript exon variant T/C snv 6.2E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs10852622
rs10852622
16 88490472 intron variant A/G snv 0.35
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs118090537
rs118090537
16 88493354 intron variant G/A snv 0.14
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs17175830
rs17175830
16 88491756 intron variant G/A;C;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1170439
rs1170439
16 68574608 intron variant T/C snv 0.78
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs56179563
rs56179563
7 130045757 intron variant G/A snv 0.28
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs6945954
rs6945954
7 139102449 intron variant G/A snv 0.31
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1109151
rs1109151
22 41356940 intron variant A/G snv 0.42
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs5758297
rs5758297
22 41324693 intron variant A/G snv 0.41
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs431978
rs431978
6 149471864 intron variant A/G snv 0.49
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs61769193
rs61769193
1 22453334 intron variant T/C snv 0.32
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs238914
rs238914
11 114113387 intron variant C/A snv 0.45
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs2846630
rs2846630
11 114086475 intron variant G/A snv 0.35
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs1811069
rs1811069
1.000 0.040 22 21627765 upstream gene variant T/A;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs2173714
rs2173714
16 69844631 intron variant C/G snv 0.39
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019