Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs317250 1.000 2 76036546 intron variant C/T snv 0.96 1
rs15705 1.000 20 6779333 3 prime UTR variant A/C;T snv 1
rs114632254 1.000 1 236482309 missense variant C/T snv 2.1E-02 2.1E-02 1
rs1444216093 1.000 4 5632031 missense variant G/A;C snv 1
rs758420403 1.000 4 5689210 missense variant A/C snv 4.0E-06 1
rs752627281 1.000 8 38419631 missense variant C/T snv 2.4E-05 6.3E-05 1
rs1292564852 1.000 4 1805414 missense variant C/T snv 7.0E-06 1
rs11806449 1.000 1 240493497 intron variant G/A snv 0.21 0.17 1
rs2268626 1.000 14 75978424 intron variant C/T snv 0.80 1
rs17015215 1.000 1 209790735 missense variant C/T snv 1
rs7802 1.000 1 209785814 3 prime UTR variant A/G snv 7.0E-04 1
rs994158401 1.000 4 4860050 missense variant A/G snv 1.4E-03 1.7E-04 1
rs777307167 1.000 2 218890128 missense variant T/C snv 1.2E-05 1
rs140920120 0.925 0.080 14 53952099 missense variant C/A;G snv 2.8E-04 2
rs483352804
EDA
0.925 0.080 X 70035389 missense variant G/A;T snv 2
rs861019 0.925 0.120 1 209802041 splice region variant A/G snv 0.44 2
rs104894469 0.925 0.080 14 36663043 missense variant G/A;T snv 4.0E-06 2
rs1095 0.925 0.080 4 4863211 3 prime UTR variant C/T snv 1.5E-02 2
rs28933970 0.925 0.080 14 36662954 missense variant T/C snv 2
rs11001553 0.925 0.080 10 52313141 intron variant C/T snv 0.12 2
rs1315861554 0.925 0.120 18 3457392 missense variant C/T snv 4.0E-06 2
rs61735045 0.882 0.160 9 134750808 missense variant G/A snv 3.5E-02 3.1E-02 3
rs104894562 0.882 0.200 17 28529157 stop gained C/T snv 4.0E-06 7.0E-06 3
rs771803303 0.882 0.160 20 38148005 missense variant G/A;C;T snv 1.6E-05; 4.1E-06 3
rs116998555 0.882 0.080 2 218890118 missense variant C/A;T snv 4.0E-06; 1.9E-03 3