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: rs28673728
rs28673728 		1 37943401 intron variant A/G snv 0.40
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs28673728
rs28673728 		1 37943401 intron variant A/G snv 0.40
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs28673728
rs28673728 		1 37943401 intron variant A/G snv 0.40
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs61776663
rs61776663 		1 37868905 intron variant C/T snv 9.4E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs61776663
rs61776663 		1 37868905 intron variant C/T snv 9.4E-02
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: rs61776678
rs61776678 		1.000 0.040 1 37911349 intron variant G/A snv 0.32
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs773387490
rs773387490 		1.000 0.120 1 37945756 missense variant G/A snv 2.4E-05 1.4E-05
CUI: C1845167
Disease: Dent Disease 2
Dent Disease 2 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2016 2016