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: rs4764887
rs4764887
IGF1 ; LINC02456
0.925 0.080 12 102430122 intron variant G/A snv 2.2E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs4764887
rs4764887
IGF1 ; LINC02456
0.925 0.080 12 102430122 intron variant G/A snv 2.2E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2011 2011