Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10263707
rs10263707
7 151706419 intron variant T/G snv 0.31
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs10263707
rs10263707
7 151706419 intron variant T/G snv 0.31
Red cell distribution width determination
0.700 1.000 1 2019 2019