Disease: Malignant neoplasm of stomach
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs9972882
STARD3
0.925 0.080 17 39651445 intron variant A/C snv 0.66 4