Source: CURATED

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: rs10815098
rs10815098
9 4865338 intron variant C/T snv 0.24
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10815098
rs10815098
9 4865338 intron variant C/T snv 0.24
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs10974808
rs10974808
9 4840380 intron variant A/G snv 9.0E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs10974808
rs10974808
9 4840380 intron variant A/G snv 9.0E-02
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10974808
rs10974808
9 4840380 intron variant A/G snv 9.0E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs10974815
rs10974815
9 4854253 intron variant C/T snv 0.11
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs10974815
rs10974815
9 4854253 intron variant C/T snv 0.11
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12351570
rs12351570
9 4806633 intron variant C/T snv 9.2E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2018 2018
dbSNP: rs12554461
rs12554461
9 4865256 intron variant A/G snv 0.59
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs13284787
rs13284787
9 4811553 intron variant A/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs13284787
rs13284787
9 4811553 intron variant A/C;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs13300663
rs13300663
9 4814948 intron variant G/A;C snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs13300663
rs13300663
9 4814948 intron variant G/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs13300663
rs13300663
9 4814948 intron variant G/A;C snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 1 2011 2011
dbSNP: rs15583
rs15583
9 4860300 3 prime UTR variant A/G snv 0.67 0.64
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs159432
rs159432
1.000 0.040 9 4844459 intron variant G/A snv 0.34
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17803780
rs17803780
9 4849647 intron variant T/C snv 0.19
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs17803780
rs17803780
9 4849647 intron variant T/C snv 0.19
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs1887430
rs1887430
9 4856234 intron variant G/A snv 0.56
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs2236496
rs2236496
9 4844265 intron variant T/C snv 0.19
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs2236496
rs2236496
9 4844265 intron variant T/C snv 0.19
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2010 2010
dbSNP: rs2236496
rs2236496
9 4844265 intron variant T/C snv 0.19
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2010 2010
dbSNP: rs2236496
rs2236496
9 4844265 intron variant T/C snv 0.19
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2236497
rs2236497
9 4844704 intron variant T/C snv 0.22 0.19
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2236497
rs2236497
9 4844704 intron variant T/C snv 0.22 0.19
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009