Source: ALL
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: rs12193797
rs12193797
6 41780614 5 prime UTR variant A/G snv 0.10
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs13193974
rs13193974
6 41782158 intron variant T/C snv 0.75
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6905726
rs6905726
6 41783074 intron variant T/C snv 0.56
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs6905726
rs6905726
6 41783074 intron variant T/C snv 0.56
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6925777
rs6925777
6 41783084 intron variant C/T snv 0.51
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs6925777
rs6925777
6 41783084 intron variant C/T snv 0.51
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs9394831
rs9394831
6 41785346 synonymous variant C/T snv 0.21 0.19
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs9394831
rs9394831
6 41785346 synonymous variant C/T snv 0.21 0.19
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009