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: rs10224002
rs10224002
0.925 0.080 7 151717955 intron variant A/G snv 0.31
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.800 1.000 1 2009 2009
dbSNP: rs10224002
rs10224002
0.925 0.080 7 151717955 intron variant A/G snv 0.31
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.800 1.000 1 2009 2009
dbSNP: rs10224210
rs10224210
1.000 0.040 7 151716108 intron variant T/C snv 0.21
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.800 1.000 1 2009 2019
dbSNP: rs7805747
rs7805747
1.000 0.080 7 151710715 intron variant G/A snv 0.26
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.710 0.667 2 2010 2018
dbSNP: rs10224002
rs10224002
0.925 0.080 7 151717955 intron variant A/G snv 0.31
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE
0.700 1.000 1 2009 2009
dbSNP: rs10224002
rs10224002
0.925 0.080 7 151717955 intron variant A/G snv 0.31
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10224210
rs10224210
1.000 0.040 7 151716108 intron variant T/C snv 0.21
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10480299
rs10480299
7 151708732 intron variant T/C snv 0.26
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10480300
rs10480300
0.925 0.120 7 151708919 intron variant C/T snv 0.24
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 1 2013 2013
dbSNP: rs10480300
rs10480300
0.925 0.120 7 151708919 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: rs10480300
rs10480300
0.925 0.120 7 151708919 intron variant C/T snv 0.24
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 1 2013 2013
dbSNP: rs10480300
rs10480300
0.925 0.120 7 151708919 intron variant C/T snv 0.24
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11983465
rs11983465
7 151699885 intron variant C/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12113155
rs12113155
7 151607887 intron variant A/C;G snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12113155
rs12113155
7 151607887 intron variant A/C;G snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12113155
rs12113155
7 151607887 intron variant A/C;G snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17173197
rs17173197
1.000 0.120 7 151571834 non coding transcript exon variant C/T snv 0.34
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.700 1.000 1 2011 2011
dbSNP: rs1881626
rs1881626
7 151825722 intron variant T/C snv 0.96
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs1881626
rs1881626
7 151825722 intron variant T/C snv 0.96
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2374270
rs2374270
7 151705704 intron variant C/A snv 0.36
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6947064
rs6947064
7 151700257 intron variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6947707
rs6947707
7 151700687 intron variant A/T snv 0.29
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6947912
rs6947912
7 151700559 intron variant G/C snv 0.22
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6948449
rs6948449
7 151701047 intron variant C/T snv 0.20
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6967507
rs6967507
7 151700401 intron variant T/C snv 0.22
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012