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: rs8176644
rs8176644
9 133273734 intron variant C/T snv
Red cell distribution width determination
0.700 1.000 1 2017 2017
dbSNP: rs8176671
rs8176671
9 133266900 intron variant A/C snv
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs8176746
rs8176746
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs9411378
rs9411378
9 133270015 intron variant A/C;T snv
Red cell distribution width determination
0.700 1.000 1 2016 2016