Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113507694
DPPA3
1.000 0.040 12 7714013 intron variant A/G snv 3.2E-02 1
rs9470079
FKBP5
1.000 0.040 6 35675286 intron variant G/A snv 0.19 1
rs4713902
LOC112267956 ; FKBP5
1.000 0.040 6 35646249 intron variant T/C snv 0.21 1
rs10083466
NRXN3
1.000 0.040 14 79518375 intron variant C/A snv 0.39 1
rs1610037
ADCYAP1
0.925 0.120 18 910634 3 prime UTR variant A/G snv 0.26 2
rs2284017
CACNG2
0.925 0.120 22 36700882 intron variant T/C snv 0.44 2
rs2284018
CACNG2
0.925 0.120 22 36701519 intron variant C/G;T snv 2
rs9836592
CHDH
0.925 0.120 3 53821056 intron variant C/T snv 0.74 2
rs1938516
ERVMER61-1
0.925 0.120 1 187433789 intron variant T/A snv 5.7E-02 2
rs11199993
FGFR2
0.925 0.120 10 121531750 intron variant G/C snv 4.8E-02 2
rs12718541
FIGNL1 ; DDC
0.925 0.080 7 50482446 intron variant A/G snv 0.55 2
rs1128306
HCG9 ; HLA-A
0.925 0.120 6 29975492 non coding transcript exon variant G/A snv 0.22 2
rs3786285
IMPA2
0.925 0.120 18 12008848 intron variant A/C;G snv 2
rs613993
IMPA2
0.925 0.120 18 12028581 non coding transcript exon variant A/G snv 0.33 2
rs5750285
LOC105373021
0.925 0.120 22 36708203 intron variant C/G snv 0.51 2
rs3974590
MPPE1
0.925 0.120 18 11892846 intron variant A/G snv 0.35 2
rs593713
MPPE1
0.925 0.120 18 11887658 intron variant G/A snv 0.42 2
rs602201
MPPE1 ; GNAL
0.925 0.120 18 11882269 3 prime UTR variant T/A snv 0.34 2
rs41084
SGCD
0.925 0.120 5 156118554 intron variant A/T snv 0.45 2
rs1311223100
SLC18A1
0.925 0.120 8 20180955 frameshift variant T/- del 5.2E-06 2
rs1497020
SLC18A1
0.925 0.120 8 20144915 3 prime UTR variant G/A snv 0.75 2
rs3735835
SLC18A1
0.925 0.120 8 20164494 intron variant G/C snv 0.38 2
rs988713
SLC18A1
0.925 0.120 8 20183790 upstream gene variant C/A;T snv 2
rs6413429
SLC6A3
0.925 0.120 5 1446912 upstream gene variant C/A snv 6.1E-02 2
rs4760816
TPH2
0.925 0.120 12 71978821 intron variant C/T snv 0.58 2