Source: ALL
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: rs10876169
rs10876169
12 51389636 intron variant T/A;C snv
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs10876169
rs10876169
12 51389636 intron variant T/A;C snv
Red cell distribution width determination
0.700 1.000 1 2019 2019