Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113198678
rs113198678
8 30384102 intron variant C/T snv 5.2E-02
CUI: C0425782
Disease: Breast size
Breast size
0.700 1.000 1 2016 2016
dbSNP: rs11993146
rs11993146
8 30462021 intron variant G/A snv 0.19
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs13275869
rs13275869
8 30452819 intron variant T/C snv 0.46
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2915594
rs2915594
8 30543850 intron variant T/C snv 0.19
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2018 2018
dbSNP: rs2915607
rs2915607
8 30422400 intron variant T/C snv 0.80
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs2979470
rs2979470
8 30430756 intron variant T/C snv 0.60
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs2979488
rs2979488
8 30423114 intron variant A/G snv 0.77
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs2979489
rs2979489
8 30423317 intron variant G/A;C snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2017 2017
dbSNP: rs2979489
rs2979489
8 30423317 intron variant G/A;C snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2017 2017
dbSNP: rs2979489
rs2979489
8 30423317 intron variant G/A;C snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs2979489
rs2979489
8 30423317 intron variant G/A;C snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs2979489
rs2979489
8 30423317 intron variant G/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs2979489
rs2979489
8 30423317 intron variant G/A;C snv
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs2979531
rs2979531
8 30525496 intron variant A/G snv 0.51
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2018 2018
dbSNP: rs35091702
rs35091702
8 30421955 intron variant GAAAAAA/- delins 0.78
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs35091702
rs35091702
8 30421955 intron variant GAAAAAA/- delins 0.78
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs35320172
rs35320172
8 30442232 intron variant T/G snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs56411466
rs56411466
8 30422549 intron variant G/A snv 0.39
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.700 1.000 1 2019 2019
dbSNP: rs6468341
rs6468341
8 30421839 intron variant T/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019