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: rs12201698
rs12201698
6 42069610 intron variant T/C snv 8.3E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs12524651
rs12524651
6 42087094 3 prime UTR variant A/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs2492943
rs2492943
6 42065702 intron variant C/T snv 0.42
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012