Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs33388
NR3C1
0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs1473473
TPH2
0.925 0.080 12 72010598 intron variant C/A;T snv 0.81 4
rs9839776
SOX2-OT
0.851 0.160 3 181593779 intron variant C/G;T snv 4
rs533123
OPRD1
0.882 0.160 1 28814643 intron variant G/A;C snv 3
rs11174202
TAFA2
0.925 0.040 12 61858476 intron variant A/G snv 0.49 2
rs13338499
LOC101927837
0.925 0.040 16 67486220 intron variant A/G;T snv 2
rs2834070 0.925 0.040 21 33015144 intron variant G/T snv 0.24 2
rs4825476
GRIA3
0.925 0.040 X 123307628 intron variant G/A;C snv 2
rs4869317
LNPEP
1.000 0.040 5 96956300 intron variant T/A snv 0.22 2
rs75063949
CARMIL1
0.925 0.040 6 25590813 intron variant C/G snv 0.14 2
rs929626
EBF1
0.925 0.120 5 158883623 intron variant A/G snv 0.40 2
rs10096097
LEPROTL1 ; DCTN6
1.000 0.040 8 30169582 intron variant G/A snv 0.62 1
rs11179027
TPH2
1.000 0.040 12 71983532 intron variant G/C snv 0.26 1
rs117957029
LOC105370064
1.000 0.040 12 127200688 intron variant T/C snv 1.4E-02 1
rs13125782
SORCS2
1.000 0.040 4 7426539 intron variant T/A;C;G snv 1
rs200312312
LOC105379109
1.000 0.040 5 104666645 intron variant T/C snv 0.16 1
rs2008387
MGMT
1.000 0.040 10 129650500 intron variant G/A snv 0.36 1
rs2287348
ERLEC1 ; GPR75-ASB3 ; ASB3
1.000 0.040 2 53812676 intron variant C/A;T snv 1
rs2295193
SYNE1
1.000 0.040 6 152131959 intron variant G/A;C snv 1
rs3825885
NTRK3
1.000 0.040 15 88059610 intron variant T/C snv 0.32 1
rs56156506 1.000 0.040 X 38140399 intron variant A/T snv 0.33 1