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: rs131656
rs131656
22 21563161 intron variant G/A snv 0.20
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs138665726
rs138665726
22 21563570 intron variant A/C snv 0.17
Red cell distribution width determination
0.700 1.000 1 2016 2016