Source: GWASCAT ×
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: rs10953541
rs10953541 		1.000 0.040 7 107604100 intron variant C/T snv 0.17
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.800 1.000 1 2011 2011
dbSNP: rs2189839
rs2189839 		1.000 0.040 7 107589581 intron variant A/G snv 0.72
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7778250
rs7778250 		7 107584120 intron variant C/A;G snv
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs7809950
rs7809950 		1.000 0.040 7 107597362 intron variant T/C snv 0.77
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018