Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11700812
CBS
1.000 0.160 21 43060480 missense variant C/G;T snv 1.2E-05 1
rs1170128038
CBS
1.000 0.160 21 43060460 missense variant C/T snv 4.0E-06 1
rs117687681
CBS
0.925 0.160 21 43060481 missense variant G/A snv 3.1E-03 1
rs1191141364
CBS
1.000 0.160 21 43072000 missense variant T/C snv 4.0E-06 1
rs1192581453
CBS
1.000 0.160 21 43060523 missense variant C/G;T snv 1
rs121964962
CBS
0.827 0.200 21 43062988 missense variant C/T snv 1.6E-04 1
rs121964963
CBS
0.925 0.160 21 43066260 missense variant G/A snv 4.0E-06 1
rs121964964
CBS
0.851 0.160 21 43066353 missense variant G/A;C snv 2.1E-04 1
rs121964965
CBS
0.925 0.160 21 43066279 missense variant C/T snv 2.8E-05 1
rs121964966
CBS
0.925 0.160 21 43066264 missense variant C/G;T snv 6.4E-05; 2.8E-05 1
rs121964967
CBS
0.925 0.160 21 43059299 missense variant T/C snv 1
rs121964968
CBS
1.000 0.160 21 43053920 missense variant A/G snv 1
rs121964969
CBS
0.882 0.160 21 43063931 missense variant C/T snv 8.0E-06 1
rs121964970
CBS
0.925 0.160 21 43065645 missense variant C/A;T snv 5.4E-06; 1.1E-05 1
rs121964971
CBS
0.851 0.160 21 43058215 missense variant G/A snv 1.2E-05 1
rs121964972
CBS
0.851 0.160 21 43060528 missense variant G/A snv 2.9E-05 1
rs121964973
CBS
0.851 0.160 21 43065481 missense variant G/A;T snv 6.0E-05 1
rs1339830457
CBS
1.000 0.160 21 43056884 missense variant G/A snv 1.9E-05 1
rs1347651454
CBS
0.882 0.160 21 43065653 missense variant C/T snv 5.4E-06 1
rs141502207
CBS
1.000 0.160 21 43063045 missense variant C/A;T snv 4.0E-06; 8.0E-06 1
rs1429138569
CBS
1.000 0.160 21 43065684 missense variant C/T snv 6.0E-06 1
rs1464223176
CBS
1.000 0.160 21 43065255 missense variant G/C snv 8.0E-06 1
rs148865119
CBS
0.925 0.160 21 43072048 missense variant G/A;C snv 1.5E-04; 4.0E-06 1
rs149119723
CBS
1.000 0.160 21 43063943 missense variant G/A snv 2.8E-05 1
rs1555872506
CBS
1.000 0.160 21 43058891 missense variant G/T snv 1