Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6586282
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		0.800 1.000 1 2009 2009
dbSNP: rs6586282
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv
CUI: C0373721
Disease: Selenium measurement
Selenium measurement 		0.700 1.000 1 2015 2015
dbSNP: rs6586282
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis 		0.010 1.000 1 2016 2016
dbSNP: rs6586282
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2016 2016
dbSNP: rs6586282
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2016 2016