Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057910
CYP2C9
0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs9923231
VKORC1
0.851 0.200 16 31096368 upstream gene variant C/A;G;T snv 6
rs4653436 1 225807509 upstream gene variant G/A snv 0.26 1
rs17847036
CYP2C9
10 94941917 synonymous variant G/A snv 5.7E-04 2.4E-04 1
rs4086116
CYP2C9
10 94947445 intron variant C/T snv 0.19 1
rs9332127
CYP2C9
10 94947714 intron variant G/C snv 4.6E-02 1
rs1799809
PROC
2 127418299 upstream gene variant G/A snv 0.52 1
rs17708472
VKORC1
16 31094032 non coding transcript exon variant G/A snv 0.17 1