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: 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: rs4147126
rs4147126
10 44911885 intron variant G/A;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4268464
rs4268464
10 44905633 intron variant T/A snv 0.63
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4439464
rs4439464
10 44889428 intron variant T/G snv 0.69
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4506594
rs4506594
10 44889363 intron variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
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: rs4948643
rs4948643
10 44884311 intron variant T/C snv 0.65
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4948645
rs4948645
10 44896033 intron variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4948922
rs4948922
10 44890380 intron variant A/C snv 0.69
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4948924
rs4948924
10 44890598 intron variant T/C snv 0.66
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4948925
rs4948925
10 44897007 intron variant G/A snv 0.54
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4948926
rs4948926
10 44897156 intron variant G/C snv 0.53
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs5000415
rs5000415
10 44888226 intron variant C/A;T snv 0.55
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6593447
rs6593447
10 44904787 intron variant G/A snv 0.56
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs7079573
rs7079573
10 44904958 intron variant G/A;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
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
dbSNP: rs7909074
rs7909074
10 44900391 non coding transcript exon variant G/A snv 0.53
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs879074
rs879074
10 44904605 intron variant G/A;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs879344
rs879344
10 44905219 intron variant G/C snv 0.72
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs914699
rs914699
10 44881618 intron variant A/C;G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012