STX12, syntaxin 12, 23673

N. diseases: 6; N. variants: 2
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: rs6598902
rs6598902 		0.925 0.040 1 27779198 intron variant T/C snv 0.18
CUI: C0947622
Disease: Cholecystolithiasis
Cholecystolithiasis 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs6598902
rs6598902 		0.925 0.040 1 27779198 intron variant T/C snv 0.18
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs80194822
rs80194822 		1 27783121 intron variant A/G snv 8.4E-03
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019