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: rs12946844
rs12946844
17 28843138 intron variant C/G;T snv
Red cell distribution width determination
0.700 1.000 1 2017 2017
dbSNP: rs35033748
rs35033748
17 28852572 intron variant T/C snv 0.26
Red cell distribution width determination
0.700 1.000 1 2016 2016