Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17404667
PRICKLE2
3 64288876 intron variant C/G snv 6.2E-02 1
rs741013
PRICKLE2
3 64306961 intron variant A/T snv 6.0E-02 1
rs12051548
TM4SF5
17 4779740 intron variant G/C snv 7.5E-02 1
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs16850360 4 74006728 intron variant A/G snv 4.2E-02 2
rs6506897 1.000 0.080 18 31215320 intergenic variant G/A snv 0.62 2
rs712964 22 19168604 upstream gene variant T/C snv 0.66 2
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs77934287 1.000 0.080 12 23071319 intron variant A/G;T snv 2
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs72928364
ABI3BP
1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs7804216
ACTR3C
1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 2
rs16939881
ALDH1A2 ; AQP9
15 58179780 intron variant G/C;T snv 2
rs6898559
ALDH7A1
1.000 0.080 5 126557237 intron variant G/A snv 0.66 2
rs74570061
ARL9
1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv 2