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
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs3798577
ESR1
0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs1473473
TPH2
0.925 0.080 12 72010598 intron variant C/A;T snv 0.81 4
rs10858583
LOC107984478
1.000 0.040 12 87334666 intergenic variant C/T snv 0.79 3
rs12149074
LOC105371357
1.000 0.040 16 80071969 intron variant C/A;G snv 3
rs13086738
SOX2-OT
1.000 0.040 3 181080939 intron variant A/G snv 0.21 3
rs17536211
GABRG1
1.000 0.040 4 46085716 intron variant A/C snv 0.14 3
rs1805576
FXR1
1.000 0.040 3 180949777 intron variant C/G;T snv 0.24 3
rs4148087
ABCG1
1.000 0.040 21 42202157 intron variant G/A;T snv 3
rs4854912
SOX2-OT
1.000 0.040 3 181063312 intron variant C/T snv 0.15 3
rs12475512 2 231433365 downstream gene variant G/A snv 0.47 2
rs13077017
FLNB
3 58120049 intron variant C/T snv 0.21 2
rs1356639869
LOC107986777 ; NPY
1.000 0.040 7 24289527 missense variant C/A snv 2
rs138206701
RASGRF2
5 81110747 intron variant A/G snv 1.7E-02 2
rs4869317
LNPEP
1.000 0.040 5 96956300 intron variant T/A snv 0.22 2
rs7322916
ATP8A2
13 25433839 intron variant G/A;C snv 2
rs74566133 8 133766099 regulatory region variant C/T snv 2.6E-02 2
rs7180942
NTRK3
15 88131345 intron variant T/C snv 0.56 1
rs550659379
NR3C1
0.882 0.160 5 143399780 missense variant T/C snv 4.0E-06 7.0E-06 5