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: rs17108533
rs17108533 		14 70783085 intron variant C/A;G;T snv 0.10
CUI: C0684328
Disease: Reasoning
Reasoning 		0.700 1.000 1 2011 2011
dbSNP: rs773256562
rs773256562 		1.000 0.080 14 70742519 missense variant G/A snv 8.0E-06
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs11625206
rs11625206 		0.925 0.080 14 70727436 3 prime UTR variant C/T snv 0.26
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs11625206
rs11625206 		0.925 0.080 14 70727436 3 prime UTR variant C/T snv 0.26
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012