Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555441861
FAH
1.000 0.120 15 80175060 frameshift variant -/T delins 1
rs1555441852
FAH
1.000 0.120 15 80175022 frameshift variant -/TGGCCCCTGCC delins 1
rs786204551
FAH
1.000 0.120 15 80186139 frameshift variant A/- del 1.4E-05 1
rs1555442289
FAH
1.000 0.120 15 80180122 splice acceptor variant A/C snv 1
rs370634385
FAH
1.000 0.120 15 80175058 missense variant A/C snv 1.6E-05 2.8E-05 1
rs1057517972
FAH
1.000 0.120 15 80153055 start lost A/G snv 8.0E-06 1
rs121965077
FAH
1.000 0.120 15 80181120 missense variant A/G snv 1
rs121965078
FAH
0.925 0.120 15 80173143 missense variant A/G snv 7.0E-06 1
rs1555440522
FAH
1.000 0.120 15 80159754 splice acceptor variant A/G snv 1
rs1555440603
FAH
1.000 0.120 15 80160408 splice acceptor variant A/G snv 1
rs1555441251
FAH
1.000 0.120 15 80168050 splice acceptor variant A/G snv 1
rs1555442385
FAH
1.000 0.120 15 80181040 splice acceptor variant A/G snv 1
rs121965073
FAH
1.000 0.120 15 80153101 missense variant A/G;T snv 8.0E-06; 2.8E-05 1
rs80338897
FAH
1.000 0.120 15 80172240 missense variant A/T snv 1
rs1057516684
FAH
1.000 0.120 15 80168056 frameshift variant ACTTACCAGTGGGCTACCATGGCCGTGCCTC/- delins 1
rs1057517113
FAH
1.000 0.120 15 80168087 frameshift variant C/- delins 1
rs1057517341
FAH
1.000 0.120 15 80153066 frameshift variant C/- delins 1
rs1555441703
FAH
1.000 0.120 15 80173142 frameshift variant C/- del 1
rs121965074
FAH
0.882 0.120 15 80162282 missense variant C/A snv 4.0E-06 1
rs886044640
FAH
1.000 0.120 15 80180126 stop gained C/A snv 7.0E-06 1
rs533540262
FAH
1.000 0.120 15 80172238 missense variant C/A;T snv 4.0E-06; 1.6E-05 1
rs769550316
FAH
1.000 0.120 15 80173016 stop gained C/T snv 1.2E-05 2.1E-05 1
rs779040832
FAH
1.000 0.120 15 80180188 missense variant C/T snv 1.6E-05; 4.5E-05 7.0E-06 1
rs781496816
FAH
1.000 0.120 15 80168116 stop gained C/T snv 4.0E-06 1
rs80338898
FAH
1.000 0.120 15 80173089 missense variant C/T snv 1.7E-04 5.6E-05 1