Source: ALL

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: rs117990941
rs117990941
15 41897706 3 prime UTR variant T/C snv 1.1E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12101888
rs12101888
15 41939155 intron variant C/T snv 0.34
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs12101888
rs12101888
15 41939155 intron variant C/T snv 0.34
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs12101888
rs12101888
15 41939155 intron variant C/T snv 0.34
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs1614170
rs1614170
15 41947207 intron variant T/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1704413
rs1704413
15 41972233 intron variant A/G snv 0.13 0.17
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs17739167
rs17739167
15 41942834 non coding transcript exon variant A/G snv 0.41
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs17739167
rs17739167
15 41942834 non coding transcript exon variant A/G snv 0.41
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs2250635
rs2250635
15 41969267 intron variant T/C snv 0.18
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs2250635
rs2250635
15 41969267 intron variant T/C snv 0.18
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs2250635
rs2250635
15 41969267 intron variant T/C snv 0.18
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs2250635
rs2250635
15 41969267 intron variant T/C snv 0.18
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs34180124
rs34180124
1.000 15 41908697 non coding transcript exon variant T/A snv 2.7E-02
Adverse effects, not elsewhere classified
0.700 1.000 1 2019 2019
dbSNP: rs4924590
rs4924590
15 41941475 intron variant T/A snv 0.30
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs4924590
rs4924590
15 41941475 intron variant T/A snv 0.30
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs4924590
rs4924590
15 41941475 intron variant T/A snv 0.30
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs57556178
rs57556178
15 41950690 intron variant G/A snv 9.3E-02
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2018 2018
dbSNP: rs57556178
rs57556178
15 41950690 intron variant G/A snv 9.3E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs59868192
rs59868192
15 41974064 intron variant T/A snv 9.9E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs72726027
rs72726027
15 41956628 intron variant T/C snv 0.11
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs8035074
rs8035074
15 41947581 intron variant C/T snv 0.44
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019