Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1583686 5 85922051 intergenic variant T/C snv 0.79 3
rs34531324
LINC01411
1.000 0.120 5 174435441 intron variant A/T snv 0.16 3
rs72772090
CAST
1.000 0.120 5 96700607 intron variant G/A;C snv 3
rs144983009 5 56792072 intergenic variant C/T snv 5.7E-02 2
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs4896310
LOC105378021
1.000 0.120 6 138018697 intergenic variant A/G;T snv 3
rs185355701
LOC105375026 ; LINC01016
6 33893066 intron variant G/A;T snv 2
rs201022 6 6669940 intergenic variant C/A;T snv 2
rs2109505
ABCB4
0.851 0.200 7 87450090 splice region variant T/A snv 0.21 0.22 6
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02 3
rs13247499
JAZF1
7 28139639 intron variant C/A snv 0.10 2
rs7803882 7 55869748 intergenic variant T/A;C snv 2
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs200088103
GPT ; LOC101928953
8 144505033 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 1.0E-04 2
rs1998303 9 82800066 intergenic variant A/G snv 0.37 3
rs111532669
PTCH1
9 95446682 3 prime UTR variant C/T snv 1.8E-02 2
rs1658972 9 6665010 intron variant C/A;T snv 2
rs2383733 9 27869512 intergenic variant A/G;T snv 2
rs4979372
AKNA
9 114377802 intron variant T/C;G snv 2
rs11597390 10 100101678 downstream gene variant G/A snv 0.29 4
rs10883437 1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43 3
rs10787429
GPAM
10 112189906 intron variant T/A;C snv 2
rs45587331
PIK3AP1
10 96700824 non coding transcript exon variant G/A snv 0.13 2
rs754465
DLG5
10 77920756 intron variant C/A snv 0.52 2