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: rs6568571
rs6568571
6 109292049 intron variant A/C;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.800 1.000 2 2009 2017
dbSNP: rs9374080
rs9374080
6 109295217 intron variant T/C snv 0.40
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.800 1.000 2 2009 2017
dbSNP: rs9400273
rs9400273
6 109311596 intron variant A/G snv 0.40
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.800 1.000 2 2009 2017
dbSNP: rs13210693
rs13210693
1.000 0.040 6 109277761 intron variant G/A snv 0.61
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.800 1.000 1 2011 2011
dbSNP: rs884366
rs884366
6 109252892 intron variant G/A snv 0.25
High density lipoprotein measurement
0.700 1.000 2 2016 2017
dbSNP: rs9386791
rs9386791
6 109287294 intron variant C/T snv 0.51
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 2 2012 2013
dbSNP: rs9400273
rs9400273
6 109311596 intron variant A/G snv 0.40
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 2 2017 2018
dbSNP: rs1006081
rs1006081
6 109304347 intron variant T/A;C snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1008084
rs1008084
6 109305762 intron variant G/A snv 0.40
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs1008084
rs1008084
6 109305762 intron variant G/A snv 0.40
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1008084
rs1008084
6 109305762 intron variant G/A snv 0.40
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2012 2012
dbSNP: rs1111863
rs1111863
6 109290003 non coding transcript exon variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1111865
rs1111865
6 109289660 intron variant C/T snv 0.51
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1111866
rs1111866
6 109289643 intron variant G/T snv 0.51
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11153165
rs11153165
6 109300956 intron variant G/A snv 0.30
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11153166
rs11153166
6 109301291 intron variant A/G snv 0.30
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11153167
rs11153167
6 109301379 intron variant A/T snv 0.31
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11153168
rs11153168
6 109308217 non coding transcript exon variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11153169
rs11153169
6 109322318 intron variant G/T snv 0.29
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs117368522
rs117368522
6 109255740 intron variant G/A snv 5.0E-04
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2017 2017
dbSNP: rs11759269
rs11759269
6 109319285 intron variant A/G snv 0.29
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11962354
rs11962354
6 109174989 intron variant C/T snv 0.12
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11964178
rs11964178
6 109240832 intron variant A/G snv 0.48
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11966072
rs11966072
6 109313625 intron variant A/G snv 0.26
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2010 2010
dbSNP: rs11966072
rs11966072
6 109313625 intron variant A/G snv 0.26
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2010 2010