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: rs4791641
rs4791641 		17 8257831 missense variant C/T snv 0.43 0.41
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2016 2017
dbSNP: rs10468482
rs10468482 		17 8259502 intron variant T/C snv 0.70
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs4791641
rs4791641 		17 8257831 missense variant C/T snv 0.43 0.41
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs4791641
rs4791641 		17 8257831 missense variant C/T snv 0.43 0.41
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4791641
rs4791641 		17 8257831 missense variant C/T snv 0.43 0.41
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs78296773
rs78296773 		17 8264644 intron variant G/A;T snv 3.2E-04; 0.16
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs9891699
rs9891699 		17 8253992 missense variant C/T snv 0.75 0.70
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019