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: rs2360748
rs2360748
19 10582948 intron variant T/C snv 0.25
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs2885056
rs2885056
19 10582952 intron variant C/A;T snv
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs7252007
rs7252007
19 10577081 intron variant T/C snv 0.90
Red cell distribution width determination
0.700 1.000 1 2017 2017