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: rs10929732
rs10929732
1.000 0.080 2 11343366 intron variant A/G snv 0.72
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs10929732
rs10929732
1.000 0.080 2 11343366 intron variant A/G snv 0.72
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2008 2008