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: rs6918289
rs6918289
0.925 0.040 6 41134089 intron variant G/T snv 9.8E-02
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 1.000 1 2018 2018
dbSNP: rs6918289
rs6918289
0.925 0.040 6 41134089 intron variant G/T snv 9.8E-02
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 1.000 1 2018 2018