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: rs8084309
rs8084309
18 46172027 upstream gene variant T/C;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs7234695
rs7234695
18 46182216 intron variant T/A snv 0.35
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs144667737
rs144667737
18 46189157 intron variant G/A snv 1.1E-02
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs144667737
rs144667737
18 46189157 intron variant G/A snv 1.1E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs8094706
rs8094706
18 46190180 intron variant T/C snv 0.62
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4890317
rs4890317
18 46190544 intron variant T/A;C snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs8086956
rs8086956
18 46193937 intron variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs9947316
rs9947316
18 46197865 intron variant T/A;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs9956574
rs9956574
18 46202237 intron variant C/T snv 0.72
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs9945783
rs9945783
18 46202294 intron variant T/C snv 0.61
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4890626
rs4890626
18 46204532 intron variant G/C;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4890628
rs4890628
18 46208079 intron variant T/C snv 0.62
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs4890628
rs4890628
18 46208079 intron variant T/C snv 0.62
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs8095374
rs8095374
18 46213522 intron variant T/C snv 0.43
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs8095374
rs8095374
18 46213522 intron variant T/C snv 0.43
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2017 2017
dbSNP: rs8095142
rs8095142
18 46213842 intron variant G/A snv 0.64
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2018 2018
dbSNP: rs8095142
rs8095142
18 46213842 intron variant G/A snv 0.64
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2018 2018
dbSNP: rs4890629
rs4890629
18 46217598 non coding transcript exon variant A/G snv 0.65
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs9675387
rs9675387
18 46218057 non coding transcript exon variant G/A snv 0.71
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4574015
rs4574015
18 46222160 intron variant T/C snv 0.73
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4542747
rs4542747
18 46222203 intron variant C/T snv 0.66
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12607898
rs12607898
18 46222812 intron variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12963943
rs12963943
18 46225695 intron variant C/T snv 0.61
Red cell distribution width determination
0.700 1.000 1 2017 2017
dbSNP: rs12963943
rs12963943
18 46225695 intron variant C/T snv 0.61
RDW - Red blood cell distribution width result
0.700 1.000 1 2017 2017
dbSNP: rs12969147
rs12969147
18 46226558 intron variant G/A snv 0.65
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012