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: rs41320847
rs41320847 		0.925 0.040 1 111507328 intron variant A/G snv 9.9E-03
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs41320847
rs41320847 		0.925 0.040 1 111507328 intron variant A/G snv 9.9E-03
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs9988442
rs9988442 		1 111554040 intron variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs746154553
rs746154553 		1.000 0.080 1 111503042 missense variant C/T snv 4.0E-06 2.1E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs1544223
rs1544223 		1.000 0.040 1 111503935 intron variant C/T snv 0.72
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs35511654
rs35511654 		0.882 0.040 1 111500165 missense variant T/G snv 9.4E-02 9.8E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs35511654
rs35511654 		0.882 0.040 1 111500165 missense variant T/G snv 9.4E-02 9.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs35511654
rs35511654 		0.882 0.040 1 111500165 missense variant T/G snv 9.4E-02 9.8E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2011 2011