Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs6354
SLC6A4
0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 16
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs4500567
TSPAN8
0.807 0.200 12 71166082 intron variant G/A;C snv 6
rs2270641
SLC18A1
0.882 0.120 8 20180955 missense variant T/C;G snv 0.32 3
rs1311223100
SLC18A1
0.925 0.120 8 20180955 frameshift variant T/- del 5.2E-06 2
rs2284018
CACNG2
0.925 0.120 22 36701519 intron variant C/G;T snv 2
rs29066
VAPA
0.925 0.120 18 9959638 3 prime UTR variant T/A;C snv 2
rs3786285
IMPA2
0.925 0.120 18 12008848 intron variant A/C;G snv 2
rs988713
SLC18A1
0.925 0.120 8 20183790 upstream gene variant C/A;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs28364997
SLC6A3
0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs61749465
MCPH1
0.851 0.120 8 6414832 missense variant A/G snv 2.1E-03 1.9E-03 5
rs78089757 0.882 0.120 10 125424260 intergenic variant G/A snv 9.9E-03 3
rs113507694
DPPA3
1.000 0.040 12 7714013 intron variant A/G snv 3.2E-02 1
rs11199993
FGFR2
0.925 0.120 10 121531750 intron variant G/C snv 4.8E-02 2
rs1938516
ERVMER61-1
0.925 0.120 1 187433789 intron variant T/A snv 5.7E-02 2
rs6413429
SLC6A3
0.925 0.120 5 1446912 upstream gene variant C/A snv 6.1E-02 2
rs4251417
SLC6A4
0.827 0.200 17 30224840 intron variant C/T snv 6.8E-02 7