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: rs2285170
rs2285170
1 172456389 intron variant C/A;G snv 3.6E-05; 0.50
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs2901656
rs2901656
1 172465672 3 prime UTR variant C/A;T snv 0.51
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs6691993
rs6691993
1 172457858 intron variant T/A;G snv
Red cell distribution width determination
0.700 1.000 1 2017 2017