Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 4
rs10513801
ETV5
3 186104564 intron variant T/G snv 9.2E-02 3
rs10767654
BDNF-AS ; LINC00678
11 27618676 intron variant T/G snv 0.73 2
rs13078960
CADM2
3 85758440 intron variant T/G snv 0.15 2
rs16886173 8 114608231 intergenic variant T/G snv 7.5E-02 2
rs7217226
SMG6 ; LOC101927839
17 2232771 intron variant T/G snv 0.38 2
rs7243357 18 59216087 upstream gene variant T/G snv 0.18 2
rs10192119
FIGN
2 163724731 intron variant T/G snv 0.28 1
rs1038088
SSH2
17 29747545 intron variant T/G snv 0.46 1
rs10799778 1 22986860 intergenic variant T/G snv 0.74 1
rs10861861 12 108042619 intergenic variant T/G snv 0.33 1
rs11047132
SOX5
12 23855501 intron variant T/G snv 9.0E-02 1
rs11608710
SOX5
12 23600993 intron variant T/G snv 5.0E-02 1
rs12522567
CWC27
5 64791196 intron variant T/G snv 0.51 1
rs12716979
STX1B
16 31000500 intron variant T/G snv 0.35 1
rs12890931
GALNT16
14 69286652 intron variant T/G snv 0.42 1
rs13062093 3 35625565 intergenic variant T/G snv 0.40 1
rs1336486
LINC00548 ; LINC00598
13 40210677 intron variant T/G snv 0.30 1
rs1522569 4 170711486 intergenic variant T/G snv 0.18 1
rs1641155
LINC01122
2 58738076 intron variant T/G snv 0.33 1
rs17014375
LINC01698
1 209370215 intron variant T/G snv 0.15 1