Source: GWASCAT

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: rs13379043
rs13379043
MIDEAS
14 73783423 intron variant T/C;G snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2017 2018
dbSNP: rs144991697
rs144991697
MIDEAS
14 73771327 intron variant G/A snv 1.6E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs145864106
rs145864106
MIDEAS
14 73778383 intron variant G/A snv 5.5E-03
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs145864106
rs145864106
MIDEAS
14 73778383 intron variant G/A snv 5.5E-03
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs533217053
rs533217053
MIDEAS
14 73741643 intron variant TCTGCAGGCTTCCGCAGCTCC/- delins 4.4E-03
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs544453779
rs544453779
MIDEAS
14 73751866 intron variant C/T snv 4.3E-03
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016