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: rs10736831
rs10736831
10 44906863 intron variant G/A snv 0.55
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2018 2018
dbSNP: rs10736831
rs10736831
10 44906863 intron variant G/A snv 0.55
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2018 2018
dbSNP: rs10793565
rs10793565
10 44892783 intron variant G/C snv 0.53
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs10793565
rs10793565
10 44892783 intron variant G/C snv 0.53
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs2281841
rs2281841
10 44911160 intron variant T/C snv 0.53
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs2281841
rs2281841
10 44911160 intron variant T/C snv 0.53
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs397731217
rs397731217
10 44904499 intron variant A/-;AA;AAA;AAAA;AAAAA delins
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs4948643
rs4948643
10 44884311 intron variant T/C snv 0.65
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs7099692
rs7099692
10 44896515 intron variant G/A;C snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs7909074
rs7909074
10 44900391 non coding transcript exon variant G/A snv 0.53
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016