Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs210962
rs210962
6 135182647 intron variant C/T snv 0.32
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.800 1.000 2 2009 2017
dbSNP: rs1022506
rs1022506
6 135190449 intron variant G/A snv 0.10
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs11154794
rs11154794
6 135194310 intron variant T/C snv 0.12 0.15
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs12660713
rs12660713
6 135196858 3 prime UTR variant G/A snv 0.10
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs12663543
rs12663543
6 135196476 intron variant A/G snv 0.16
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs17639758
rs17639758
6 135202112 intron variant G/A snv 4.4E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs3752383
rs3752383
6 135201617 intron variant A/G snv 0.11 0.11
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs6920829
rs6920829
6 135198362 intron variant T/C snv 0.14
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs6936293
rs6936293
6 135214883 intron variant C/T snv 0.17
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs7738267
rs7738267
6 135216055 intron variant A/G snv 0.17
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009