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: rs12439144
rs12439144
15 78244582 intron variant G/A snv 0.37
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12591810
rs12591810
15 78243867 intron variant A/G snv 0.37
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12904669
rs12904669
15 78244187 intron variant C/T snv 0.37
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1879154
rs1879154
15 78244813 intron variant T/A;C snv 0.37
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs1879154
rs1879154
15 78244813 intron variant T/A;C snv 0.37
RDW - Red blood cell distribution width result
0.700 1.000 1 2016 2016
dbSNP: rs1879154
rs1879154
15 78244813 intron variant T/A;C snv 0.37
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs4887023
rs4887023
15 78243095 intron variant C/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs4887023
rs4887023
15 78243095 intron variant C/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs58119220
rs58119220
15 78244894 intron variant C/G snv 0.37
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2016 2016