Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28908768
CYP3A4
1.000 7 99771177 intron variant -/CT delins 5
rs17029090
C4orf17
1.000 4 99522696 synonymous variant A/G snv 4.8E-02 8.8E-02 5
rs75122859
MBNL2 ; LOC101927385
1.000 13 97248751 intron variant A/T snv 7.0E-02 5
rs7691759 0.882 0.120 4 9686390 intron variant T/A;C snv 7
rs2514923
LINC02748
1.000 11 91221441 intron variant C/G;T snv 5
rs73649983
LOC102724057
1.000 9 85800845 intron variant C/T snv 6.8E-02 5
rs6585943 1.000 10 85322237 intergenic variant G/A snv 0.41 5
rs2953235
LINC00937
1.000 12 8336986 intron variant G/A;C snv 5
rs17160151
FBN3
1.000 19 8085509 missense variant C/T snv 1.8E-02 7.3E-02 5
rs7006546
ZNF704
1.000 8 80793161 intron variant T/C snv 0.23 5
rs72642263
LRMDA
1.000 10 76449748 intron variant A/G snv 9.2E-02 5
rs944857
TRPM6
1.000 9 74737882 intron variant A/G;T snv 5
rs150933152
CLEC18B
1.000 16 74411734 missense variant C/T snv 5
rs9993633
MOB1B ; DCK
1.000 4 70997893 intron variant G/A snv 0.11 5
rs28711761 1.000 8 6894170 downstream gene variant A/G snv 8.3E-02 5
rs77700841
MAGI1
1.000 3 65852193 intron variant G/C;T snv 5
rs1349596
CADPS
1.000 3 62542448 intron variant C/T snv 6.3E-02 5
rs949214
CCBE1
1.000 18 59519354 intron variant A/C snv 0.31 5
rs8094014 1.000 18 5940342 intron variant A/G snv 0.14 5
rs6742445
FANCL
1.000 2 58218738 intron variant A/T snv 7.1E-02 5
rs9992616 1.000 4 56781880 intergenic variant C/A;G snv 5
rs56775982 1.000 8 54303623 regulatory region variant C/T snv 8.5E-02 5
rs9636146
TMC4
1.000 19 54162804 intron variant G/A snv 4.1E-02 6.2E-02 5
rs11905359
TMEM230
1.000 20 5079306 intron variant C/A snv 7.1E-02 5
rs79272944
ZBTB7C
1.000 18 48131482 intron variant G/T snv 6.7E-02 5