Source: GWASDB

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: rs7775698
rs7775698
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.800 1.000 3 2009 2013
dbSNP: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination
0.800 1.000 3 2007 2015
dbSNP: rs1547247
rs1547247
6 135069698 intron variant G/A snv 0.22
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.800 1.000 2 2009 2019
dbSNP: rs7775698
rs7775698
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
Finding of Mean Corpuscular Hemoglobin
0.800 1.000 2 2009 2013
dbSNP: rs7775698
rs7775698
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 2 2010 2012
dbSNP: rs7775698
rs7775698
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.800 1.000 2 2009 2012
dbSNP: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 2 2009 2019
dbSNP: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.800 1.000 2 2009 2018
dbSNP: rs7745098
rs7745098
1.000 0.120 6 135093866 intron variant C/G;T snv
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.800 1.000 1 2013 2013
dbSNP: rs7775698
rs7775698
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.800 1.000 1 2010 2012
dbSNP: rs7776054
rs7776054
6 135097778 intron variant A/G snv 0.24
Finding of Mean Corpuscular Hemoglobin
0.800 1.000 1 2009 2018
dbSNP: rs7776054
rs7776054
6 135097778 intron variant A/G snv 0.24
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 1 2012 2018
dbSNP: rs9373124
rs9373124
6 135102071 intron variant T/C snv 0.33
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.800 1.000 1 2011 2011
dbSNP: rs9373124
rs9373124
6 135102071 intron variant T/C snv 0.33
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 1 2009 2012
dbSNP: rs9376090
rs9376090
6 135090090 intron variant T/C snv 0.19
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 1 2012 2017
dbSNP: rs9376090
rs9376090
6 135090090 intron variant T/C snv 0.19
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.800 1.000 1 2009 2018
dbSNP: rs9376090
rs9376090
6 135090090 intron variant T/C snv 0.19
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2013 2018
dbSNP: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
Finding of Mean Corpuscular Hemoglobin
0.800 1.000 1 2013 2013
dbSNP: rs1014021
rs1014021
6 135013462 intron variant A/G snv 0.53
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1041480
rs1041480
6 135051938 intron variant G/T snv 0.46
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10484496
rs10484496
6 134978544 intron variant T/C snv 0.31
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1074849
rs1074849
6 135102274 intron variant G/A snv 0.21
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1074849
rs1074849
6 135102274 intron variant G/A snv 0.21
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs10872427
rs10872427
6 135032314 intron variant T/C;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11154791
rs11154791
6 135058010 intron variant A/G snv 0.33
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012