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: rs5279
rs5279
PTGS2
0.925 0.080 1 186675946 missense variant A/C;G;T snv 4.0E-06; 4.5E-03; 8.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs5279
rs5279
PTGS2
0.925 0.080 1 186675946 missense variant A/C;G;T snv 4.0E-06; 4.5E-03; 8.0E-06
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2009 2009