Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs200855945
SSPN ; BHLHE41
0.925 0.040 12 26124961 5 prime UTR variant ACACGCACAC/-;ACACGCACACACACGCACAC delins 1.6E-02 3
rs201203751
FYB1
0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3
rs201569130 0.925 0.040 6 1402916 intergenic variant GACA/- delins 1.1E-02 3
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs2919375
NRG1
0.925 0.040 8 32719327 intron variant G/A snv 0.77 3
rs2979204 0.925 0.040 8 8441347 regulatory region variant T/C snv 0.34 3
rs2984618
TAL1
0.925 0.040 1 47224766 intron variant G/T snv 0.52 3
rs34102224 0.925 0.040 8 5364506 downstream gene variant G/C snv 0.12 3
rs34177316
LOC107986273 ; APBB2
0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3
rs352759
TUSC3
0.925 0.040 8 15742205 intron variant T/A snv 3
rs35792458
XKR6
0.925 0.040 8 10964921 intron variant G/C snv 0.53 3
rs4761545 0.925 0.040 12 94032692 regulatory region variant G/T snv 0.56 3
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs55679149
LOC105378841
0.925 0.040 1 89068655 upstream gene variant C/T snv 0.34 3
rs56388524 0.925 0.040 5 45757459 intergenic variant C/A;T snv 2.0E-02 3
rs5743467
DEFB1
0.925 0.040 8 6874007 intron variant C/G snv 0.19 3
rs6063349
CSE1L
0.925 0.040 20 49065345 intron variant G/A;C;T snv 3
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs7189979
SNX29
0.925 0.040 16 12536330 intron variant A/C;G;T snv 3
rs73425402
NAV3
0.925 0.040 12 77503518 intron variant T/A snv 4.1E-02 3
rs74860738 0.925 0.040 11 80671683 intergenic variant G/A snv 7.2E-02 3
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs77945277
BAZ1A
0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3