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: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 5 2009 2019
dbSNP: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination
0.800 1.000 2 2007 2015
dbSNP: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.800 1.000 2 2009 2018
dbSNP: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
Finding of Mean Corpuscular Hemoglobin
0.800 1.000 1 2013 2013
dbSNP: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0474543
Disease: Hemoglobin A2 measurement
Hemoglobin A2 measurement
0.700 1.000 1 2013 2013
dbSNP: rs9399137
rs9399137
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2015 2015