Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10061469 5 73222321 intron variant T/C snv 0.37 1
rs10142466 14 68805067 intergenic variant A/C;G;T snv 1
rs10521318 16 85977731 intron variant C/G;T snv 1
rs11187157 10 92742487 TF binding site variant T/C snv 0.40 1
rs11641016 16 85981275 intron variant C/G snv 0.18 1
rs11677953 2 218256940 non coding transcript exon variant G/A snv 0.36 1
rs12585310 13 26954210 intergenic variant G/A snv 0.27 1
rs1388585 12 40137889 downstream gene variant G/A snv 0.95 1
rs149169037 7 20537675 intergenic variant G/A snv 5.5E-02 1
rs17000400 4 75251521 regulatory region variant C/T snv 0.12 1
rs2427870 X 136581905 upstream gene variant C/T snv 0.52 1
rs2472649 4 73991991 upstream gene variant A/G;T snv 1
rs2839073 21 45953845 regulatory region variant T/C snv 0.16 1
rs2847278 18 12778716 upstream gene variant C/T snv 0.83 1
rs4836519 5 130681594 intron variant T/A;C snv 1
rs4899554 14 75234518 downstream gene variant C/T snv 0.14 1
rs6935723 6 32713892 upstream gene variant T/C snv 0.29 1
rs72634258 1 8090578 intron variant T/C snv 0.13 1
rs7547569 1 67265685 downstream gene variant T/C snv 4.7E-02 1
rs7911264 10 92677094 intergenic variant T/A;C;G snv 1
rs7968307 12 114620647 upstream gene variant T/C snv 0.33 1
rs8009169 14 42813211 intergenic variant G/C snv 0.78 1
rs9313808 5 159393836 intron variant A/G snv 0.89 1
rs950318 3 80354036 intergenic variant C/G snv 0.22 1
rs6545800
ADCY3
2 24896016 intron variant C/T snv 0.53 1