Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs13306698 0.882 0.240 7 95311470 missense variant T/C snv 6.0E-03 1.9E-03 3
rs781071878 1.000 0.040 7 95311484 missense variant T/C snv 4.2E-04 1.0E-04 1
rs755603793 0.925 0.080 7 95308077 missense variant C/T snv 1.6E-05 2
rs765657236 1.000 0.120 7 95318360 synonymous variant G/A snv 8.0E-06 1
rs771025483 1.000 0.040 7 95306310 missense variant G/C snv 4.0E-06 1
rs705382 0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs757158 0.851 0.240 7 95326216 upstream gene variant C/T snv 0.58 5
rs3735590 0.925 0.080 7 95298183 3 prime UTR variant G/A snv 0.14 3
rs1302207706 1.000 0.080 7 95316748 missense variant C/T snv 2
rs2057681 7 95308945 intron variant A/G snv 0.43 2
rs705379 1.000 0.080 7 95324583 upstream gene variant G/A;C;T snv 2
rs705381 1.000 0.080 7 95324637 upstream gene variant T/C snv 0.72 2
rs72552787 0.925 0.080 7 95315388 missense variant T/C snv 2
rs854566 0.925 0.080 7 95319437 intron variant A/G snv 0.78 2
rs11292716 7 95305887 intron variant A/- delins 1
rs1157745 7 95311726 intron variant G/T snv 0.42 1
rs2074351 1.000 0.080 7 95318487 non coding transcript exon variant G/A snv 0.26 1
rs2237583 7 95320865 intron variant C/G;T snv 1
rs3917481 1.000 0.040 7 95321453 intron variant C/T snv 3.7E-02 1
rs3917502 7 95316432 intron variant C/T snv 3.9E-02 1
rs3917510 7 95313808 intron variant T/G snv 6.2E-02 1
rs3917532 7 95310807 intron variant A/T snv 0.42 1
rs3917539 7 95308384 intron variant -/AA delins 0.42 1