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: rs3785309
rs3785309
16 162650 intron variant C/T snv 0.10
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs7194649
rs7194649
16 165107 non coding transcript exon variant C/A snv 0.18
Red cell distribution width determination
0.700 1.000 1 2017 2017