Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3757441
EZH2
0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs267601395
EZH2
0.925 0.160 7 148811636 missense variant A/G;T snv 7
rs41277434
EZH2
0.851 0.160 7 148809304 splice region variant A/C;G snv 6.8E-02; 8.0E-06 6
rs887569
EZH2
0.882 0.120 7 148808210 intron variant C/T snv 0.73 5
rs2302427
EZH2
1.000 0.080 7 148828812 missense variant C/G snv 7.8E-02 6.0E-02 4