Source: BEFREE

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: rs7853122
rs7853122
RAPGEF1
0.925 0.080 9 131705224 intron variant C/T snv 0.87
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2011 2011
dbSNP: rs7853122
rs7853122
RAPGEF1
0.925 0.080 9 131705224 intron variant C/T snv 0.87
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs7853122
rs7853122
RAPGEF1
0.925 0.080 9 131705224 intron variant C/T snv 0.87
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2011 2011