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: rs7832552
rs7832552 		8 109103447 intron variant C/T snv 0.29
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.800 1.000 1 2009 2009
dbSNP: rs12544197
rs12544197 		8 109095596 intron variant G/A;C snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs16892496
rs16892496 		1.000 0.080 8 109097622 intron variant A/C;G;T snv
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2009 2009
dbSNP: rs16892496
rs16892496 		1.000 0.080 8 109097622 intron variant A/C;G;T snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs771222349
rs771222349 		1.000 0.040 8 109087904 missense variant T/A;C snv 4.0E-06; 8.0E-06
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.010 1.000 1 2017 2017