Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs11080055 0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs1142 0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs114254831 0.827 0.040 6 32187804 intron variant A/G snv 5
rs116503776 0.827 0.040 6 31962685 intron variant G/A snv 5
rs11884770 0.851 0.040 2 227222204 intron variant T/A;C snv 4
rs12019136 0.851 0.040 19 5835666 intron variant G/A snv 0.12 4
rs12357257 0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs12661281 0.882 0.040 6 31874821 missense variant T/A snv 0.15 0.11 3
rs13095226 0.851 0.040 3 99677428 intron variant T/C snv 9.5E-02 5
rs140647181 0.851 0.040 3 99461824 intergenic variant T/C snv 1.5E-02 4
rs141853578
CFI
0.807 0.040 4 109764664 missense variant C/T snv 4.2E-04 3.9E-04 6
rs142450006 0.851 0.040 20 45986353 regulatory region variant TTCT/-;TTCTTTCT delins 2.0E-02 4
rs147859257
C3
0.827 0.040 19 6718135 missense variant T/G snv 2.8E-03 2.4E-03 6
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs17231506 0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 10
rs181705462 0.851 0.040 6 31979250 intron variant G/C;T snv 4
rs187328863 0.851 0.040 1 196411028 intron variant C/T snv 1.6E-02 4
rs191281603 0.851 0.040 1 196989521 intron variant C/G;T snv 4.6E-03 4
rs1999930
FRK
0.882 0.040 6 116065971 intergenic variant C/A;G;T snv 3
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs2284665 0.882 0.040 10 122467114 intron variant G/A;T snv 3
rs2285714 0.882 0.040 4 109717654 synonymous variant C/T snv 0.37 0.31 3