Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs486907
RNASEL
0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs1799977
MLH1
0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs138213197
HOXB13
0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs3803185
ARL11
0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs536562413
FBXO11 ; MSH6
0.732 0.240 2 47799934 missense variant A/G snv 1.2E-05 7.0E-06 15
rs74315364
RNASEL
0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs627928
RNASEL
0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10
rs4792311
ELAC2
0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 9
rs5030739
ELAC2
0.776 0.160 17 12996585 missense variant C/T snv 3.5E-02 2.9E-02 8
rs35831931
MLH1
0.882 0.120 3 37050528 missense variant G/A;T snv 1.2E-03; 2.0E-05 4
rs63750109
MLH1
0.882 0.120 3 37048559 missense variant G/A;T snv 1.1E-04; 4.0E-06 3
rs1114167843
MSH2
0.882 0.120 2 47478396 missense variant A/C;G snv 3