Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1130183 0.827 0.160 1 160041722 missense variant G/A snv 4.6E-02 4.7E-02 6
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs113994097 0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs1162306056 0.882 0.080 8 132174294 missense variant C/T snv 5
rs11663316 1.000 0.040 18 9027916 intergenic variant T/A snv 0.34 2
rs117067974 0.851 0.080 20 63414174 missense variant C/A;G snv 2.0E-05; 2.6E-03 5
rs1178326 1.000 0.040 7 18195234 intron variant T/C snv 3.9E-02 2
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs118166657 1.000 0.040 14 63580544 intergenic variant C/G snv 1.3E-02 2
rs118192211 0.790 0.080 20 63439644 missense variant G/A;C snv 9
rs118192249 0.882 0.080 8 132175461 missense variant A/G snv 4.0E-06 3
rs119488099 0.925 0.120 10 93777592 missense variant C/T snv 1.4E-05 3
rs12059546 0.925 0.040 1 239806797 intron variant A/G snv 0.30 2
rs121434610
SMS
0.882 0.120 X 21967312 missense variant G/A snv 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908165 0.925 0.120 1 154273538 stop gained C/G;T snv 1.6E-05 4
rs121908225 0.790 0.120 19 13365448 missense variant G/A snv 12
rs121908230 0.882 0.080 19 13262789 missense variant C/T snv 5
rs121908869 0.882 0.160 14 80955802 missense variant G/C snv 4.0E-05 7.0E-06 5
rs121909674 0.790 0.080 5 162153132 stop gained C/T snv 8
rs121909731 0.851 0.120 10 87057692 missense variant G/A;C snv 4.0E-06 7
rs121912504 0.851 0.200 7 150951711 missense variant G/A snv 6
rs121912707 0.925 0.040 5 126552059 missense variant C/G snv 3.6E-04 2.4E-04 3
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480