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: rs1023741
rs1023741 		1.000 0.080 10 96663139 intron variant T/C snv 0.14
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
Secondary malignant neoplasm of colon and/or rectum 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs4320890
rs4320890 		1.000 0.080 10 96625050 intron variant C/G;T snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs45587331
rs45587331 		10 96700824 non coding transcript exon variant G/A snv 0.13
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs45587331
rs45587331 		10 96700824 non coding transcript exon variant G/A snv 0.13
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2018 2018