Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs11153730 6 118346359 intergenic variant T/C snv 0.40 4
rs13165478 5 154489480 upstream gene variant G/A snv 0.41 3
rs10850409 12 114943935 intergenic variant G/A snv 0.27 2
rs12036340 1 162045950 intergenic variant A/G snv 0.24 2
rs1362212 7 35265695 intergenic variant G/A snv 0.11 2
rs17391905 1 51080468 intergenic variant T/G snv 3.7E-02 2
rs7784776 7 46580547 intergenic variant A/G snv 0.42 2
rs9851724 3 38678444 intergenic variant C/T snv 0.73 2
rs12039739 1 115790490 regulatory region variant C/T snv 0.28 1
rs13185595 5 154492610 upstream gene variant G/A snv 0.41 1
rs1344852 4 20182314 intergenic variant G/A;C;T snv 1
rs1419856 7 35267372 intergenic variant A/G snv 0.11 1
rs4708832 6 159472905 intron variant G/T snv 0.31 1
rs6968945 7 46601302 intergenic variant C/T snv 0.61 1
rs7132327 12 114943266 intergenic variant T/C snv 0.27 1
rs7771320 6 7502516 upstream gene variant T/C snv 5.4E-02 1
rs7909027
CACNB2
10 18406963 intron variant T/C snv 0.44 1
rs1562782
CAND1.11 ; AMPD3
11 10321164 intron variant A/C;G snv 1
rs4642101
CAND2
1.000 0.080 3 12800724 intron variant T/G snv 0.63 3
rs3929778
CASC20
20 6479643 intron variant C/T snv 0.84 1
rs4074536
CASQ2
1 115768346 missense variant T/C snv 0.33 0.34 2
rs7537765
CLCN6
1 11827246 intron variant A/G snv 0.15 0.18 1
rs359466
CPEB4
5 173888863 5 prime UTR variant C/G snv 0.11 1