Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11374964 1.000 0.080 11 108474788 3 prime UTR variant -/A ins 2.4E-05; 0.47 0.43 1
rs111307654 1.000 0.080 7 94655777 intron variant -/AA;AAA;AAAA delins 1
rs10644111 1.000 0.080 7 92022864 protein altering variant -/AAC delins 0.39 0.46 1
rs16342 1.000 0.080 4 1983005 3 prime UTR variant -/AACA;ACA delins 1
rs483353122 0.851 0.200 13 32363410 frameshift variant -/AG ins 4
rs1114167628 0.925 0.080 10 87961033 stop gained -/ATATCTAG delins 5
rs138060088 1.000 0.080 5 44933882 intergenic variant -/ATG delins 0.46 1
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs886040340 0.882 0.080 13 32319111 frameshift variant -/C delins 4
rs28360317 0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs11283943
MCC
0.882 0.160 5 113071088 splice donor variant -/CGCACTGTCTTCCT;CGCGCTGTCTTCCT;CGTGCTGTCTTCCT delins 4
rs143072280 1.000 0.080 10 38105003 intron variant -/CTTT delins 0.40 1
rs80357906 0.827 0.200 17 43057062 frameshift variant -/G delins 1.8E-04 8
rs113289039 1.000 0.080 6 166087861 intergenic variant -/G delins 0.35 1
rs3215401 1.000 0.080 5 1296140 upstream gene variant -/G delins 0.25 1
rs11462858 1.000 0.080 10 121334477 intergenic variant -/T delins 0.40 1
rs35522438 1.000 0.080 7 92243558 intron variant -/T delins 0.40 1
rs56077980
FTO
1.000 0.080 16 54107654 intron variant -/T delins 0.26 1
rs3215684 0.925 0.080 20 50578329 intron variant -/T;TC ins 0.62 2
rs70991108 0.807 0.280 5 80654344 intron variant -/TCGCGCGTCCCGCCCAGGT;TGGCGCGTCCCGCCCAGGT ins 0.51 6
rs1414323823 0.851 0.160 15 74722772 frameshift variant -/TCTCGGT ins 4.0E-06 4
rs113211432 0.882 0.080 2 214767532 frameshift variant -/TG delins 3
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs10623258 1.000 0.080 14 104745924 non coding transcript exon variant -/TT ins 0.56 1
rs78579487 1.000 0.080 3 156800879 intron variant -/TT delins 0.55 1