Source: GWASDB

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: rs7385804
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.800 1.000 1 2009 2009
dbSNP: rs7385804
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65
CUI: C0428578
Disease: Iron level result
Iron level result 		0.700 1.000 1 2011 2011
dbSNP: rs7385804
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65
CUI: C0337439
Disease: Iron measurement
Iron measurement 		0.700 1.000 1 2011 2011
dbSNP: rs7385804
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2009 2009
dbSNP: rs7385804
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012