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: rs28673728
rs28673728
1 37943401 intron variant A/G snv 0.40
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs61776663
rs61776663
1 37868905 intron variant C/T snv 9.4E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019