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: rs2068229
rs2068229 		3 141904462 intron variant A/G snv 0.35
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 3 2016 2019
dbSNP: rs2068229
rs2068229 		3 141904462 intron variant A/G snv 0.35
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 3 2016 2019
dbSNP: rs3804772
rs3804772 		3 141915214 intron variant G/A snv 8.7E-02
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs6782694
rs6782694 		3 141909018 intron variant C/A snv 0.14
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019