Source: GWASCAT

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: rs2075672
rs2075672
7 100642673 intron variant A/G snv 0.65
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 1 2012 2016
dbSNP: rs2075672
rs2075672
7 100642673 intron variant A/G snv 0.65
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 3 2012 2017
dbSNP: rs10953299
rs10953299
7 100645788 intron variant T/C snv 0.21
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2018 2018
dbSNP: rs2075672
rs2075672
7 100642673 intron variant A/G snv 0.65
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs2075672
rs2075672
7 100642673 intron variant A/G snv 0.65
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2017 2017
dbSNP: rs2075672
rs2075672
7 100642673 intron variant A/G snv 0.65
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2017 2017
dbSNP: rs2075672
rs2075672
7 100642673 intron variant A/G snv 0.65
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs2075672
rs2075672
7 100642673 intron variant A/G snv 0.65
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2017 2017
dbSNP: rs2075672
rs2075672
7 100642673 intron variant A/G snv 0.65
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs7383856
rs7383856
7 100644788 intron variant G/A snv 4.9E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2018 2018