Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs201203751
FYB1
0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 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
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 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
rs77945277
BAZ1A
0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3
rs80278479
TFAP2D
0.925 0.040 6 50758466 intron variant C/G snv 3.0E-03 3
rs9321987
UTRN
0.925 0.040 6 144709148 intron variant C/T snv 0.40 3
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs116609693
ANKRD19P
0.925 0.040 9 92811394 intron variant C/T snv 6.1E-02 2
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 2
rs1690818
CNTN5
0.925 0.040 11 99625823 intron variant C/T snv 0.61 2
rs17156280
CACNA2D1
0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02 2
rs2017122
KMT2A
0.925 0.040 11 118444134 intron variant C/T snv 4.0E-02 2
rs2221540
OPCML
0.925 0.040 11 132846474 intron variant A/G snv 0.11 2
rs319924
EYS ; PHF3
0.925 0.040 6 63777354 intron variant A/G;T snv 2
rs62100776
DCC
0.925 0.040 18 53228263 intron variant A/T snv 0.35 2