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: rs1977080
rs1977080
22 43934151 intron variant C/T snv 0.19
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2018 2018
dbSNP: rs2294915
rs2294915
1.000 0.040 22 43945024 intron variant C/G;T snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs738409
rs738409
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019