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: rs4794333
rs4794333 		1.000 0.040 17 47968129 intron variant T/C snv 0.35
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs886444
rs886444 		17 47974545 non coding transcript exon variant G/A snv 0.34 0.35
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs2737
rs2737 		0.851 0.080 17 47981705 missense variant T/C snv 0.25 0.19
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs2737
rs2737 		0.851 0.080 17 47981705 missense variant T/C snv 0.25 0.19
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs2737
rs2737 		0.851 0.080 17 47981705 missense variant T/C snv 0.25 0.19
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2011 2011
dbSNP: rs2737
rs2737 		0.851 0.080 17 47981705 missense variant T/C snv 0.25 0.19
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2011 2011