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: rs11082518
rs11082518
18 46262069 intron variant G/A snv 0.61
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12605945
rs12605945
18 46254155 intron variant A/G;T snv
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: rs12962307
rs12962307
18 46235454 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
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: rs3744858
rs3744858
18 46265306 3 prime UTR variant C/T snv 0.61
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs3744858
rs3744858
18 46265306 3 prime UTR variant C/T snv 0.61
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs4542747
rs4542747
18 46222203 intron variant C/T snv 0.66
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: rs4890317
rs4890317
18 46190544 intron variant T/A;C snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4890319
rs4890319
18 46232678 3 prime UTR variant T/A snv 0.71
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: 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: rs4890632
rs4890632
18 46246327 intron variant G/A snv 0.62
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4890633
rs4890633
18 46253312 intron variant G/A snv 0.62
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2017 2017
dbSNP: rs4890633
rs4890633
18 46253312 intron variant G/A snv 0.62
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs62098160
rs62098160
18 46252149 intron variant T/A;C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs6507691
rs6507691
18 46228682 intron variant T/C;G snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs6507693
rs6507693
18 46249171 intron variant G/A snv 0.70
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012