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: rs117268208
rs117268208 		16 69159416 intron variant C/T snv 3.2E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs5011579
rs5011579 		16 69153415 intron variant C/G snv 0.76
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs9940899
rs9940899 		16 69136024 intron variant T/C snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs119465999
rs119465999 		1.000 0.080 16 69165386 missense variant C/A;T snv 8.0E-06; 3.3E-03
CUI: C1858051
Disease: NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS
NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.020 1.000 2 2002 2013