Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11102807 1.000 0.040 1 114518963 intergenic variant A/G snv 0.44 1
rs12456492 0.882 0.080 18 43093415 intron variant A/G snv 0.33 1
rs12518194 1.000 0.040 5 25951452 intergenic variant A/G snv 0.27 1
rs1408744 1.000 0.040 6 23789887 intergenic variant A/G snv 0.63 1
rs155806 1.000 0.040 5 140970255 intron variant A/G snv 8.9E-02 1
rs263030 1.000 0.040 3 183807333 non coding transcript exon variant A/G snv 0.44 1
rs263035 1.000 0.040 3 183805869 intron variant A/G snv 0.44 1
rs409649 1.000 0.040 5 25841054 intergenic variant A/G snv 0.29 1
rs4701259 1.000 0.040 5 25900989 intergenic variant A/G snv 0.71 1
rs6053022 1.000 0.040 20 4992810 intron variant A/G snv 0.36 1
rs6537825 1.000 0.040 1 114405659 missense variant A/G snv 0.88 0.92 1
rs6752370 1.000 0.040 2 229653517 intron variant A/G snv 0.24 1
rs6891903 1.000 0.040 5 11371193 intron variant A/G snv 6.8E-02 1
rs7800565 1.000 0.040 7 16740384 TF binding site variant A/G snv 0.16 1
rs922551 1.000 0.040 5 25867431 intergenic variant A/G snv 0.28 1
rs1346536 1.000 0.040 5 25915543 downstream gene variant A/G;T snv 1
rs2710102 0.790 0.120 7 147877298 intron variant A/G;T snv 1
rs351871 1.000 0.040 5 77680214 regulatory region variant A/G;T snv 1
rs7380139 1.000 0.040 5 25926257 intergenic variant A/G;T snv 1
rs926938 1.000 0.040 1 114697195 upstream gene variant A/G;T snv 1
rs1567574466 1.000 0.040 16 89283404 stop gained A/T snv 1
rs7794745 0.851 0.040 7 146792514 intron variant A/T snv 0.49 1
rs1057518658 1.000 0.040 2 165331409 frameshift variant AC/- del 1
rs1057518345 0.742 0.400 20 50894172 frameshift variant ACTA/- delins 25
rs558269137 0.851 0.160 1 152312601 frameshift variant ACTG/- delins 1.3E-02 8