Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57408770 1.000 0.080 2 219058688 non coding transcript exon variant -/AAG delins 2
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11283943
MCC
0.882 0.160 5 113071088 splice donor variant -/CGCACTGTCTTCCT;CGCGCTGTCTTCCT;CGTGCTGTCTTCCT delins 4
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs764803020 0.851 0.040 17 7673750 frameshift variant -/TTTCCGCCGG delins 4.0E-06 5
rs17103265 0.925 0.080 14 35405503 upstream gene variant A/- delins 3
rs61734277 0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 5
rs121909174 0.925 0.120 19 17881961 missense variant A/C snv 1.2E-05 3
rs4635002 0.925 0.080 10 127064415 intron variant A/C snv 0.92 3
rs78311289 0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs1131691021 0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs17855750 0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs2682818 0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs9138 0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12
rs5999749 0.925 0.080 22 21833371 intron variant A/C;T snv 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188