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: rs12619285
rs12619285
1.000 0.040 2 212959321 intron variant A/G snv 0.31
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.800 1.000 3 2009 2019
dbSNP: rs445
rs445
7 92779056 intron variant C/T snv 0.14
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.800 1.000 3 2011 2019
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: rs113473633
rs113473633
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02
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: rs12705849
rs12705849
7 113142501 intron variant G/A snv 0.32
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs150640087
rs150640087
7 50376454 intron variant G/T snv 1.0E-02
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: 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: rs1695315
rs1695315
3 3111655 intron variant G/A snv 0.56
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
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: rs2960422
rs2960422
1.000 0.080 3 12293492 intron variant G/A snv 0.59
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs34290285
rs34290285
0.851 0.120 2 241759225 intron variant G/A snv 0.27
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs410867
rs410867
19 16316300 intron variant A/G snv 0.32
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs61612642
rs61612642
6 42229969 intron variant C/T snv 0.21
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs62408225
rs62408225
1.000 0.120 6 90246690 intron variant A/G snv 0.26
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs7288670
rs7288670
22 24225858 intron variant A/C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs73072483
rs73072483
3 50734193 intron variant G/A snv 9.6E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs7569084
rs7569084
2 65429835 intron variant C/T snv 0.62
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs9504361
rs9504361
1.000 0.040 6 577820 intron variant A/G snv 0.40
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs960709
rs960709
0.882 0.120 5 151081488 intron variant A/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs9829778
rs9829778
3 196822218 intron variant G/A snv 0.53
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs9900933
rs9900933
UNK
17 75805073 intron variant T/A;C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019