Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7624084
ZBTB38
3 141374443 intron variant T/C snv 0.54 3
rs10018902 4 120941346 intergenic variant G/A;T snv 2
rs10198628 2 12824371 intron variant A/G snv 0.59 2
rs11030102
BDNF ; BDNF-AS
11 27660049 non coding transcript exon variant C/G snv 0.19 2
rs112540634
ILRUN
6 34656128 intron variant C/G;T snv 2
rs116975424
RFX3
9 3518833 intron variant T/C snv 2.6E-02 2
rs12625495
ZNF341
20 33775731 intron variant G/A;C;T snv 2
rs144582188 4 45163634 intergenic variant CTT/- delins 2
rs146144484 6 3865792 intron variant C/G;T snv 2
rs1650505 5 158602726 intergenic variant G/A snv 0.22 2
rs17668565 5 92818872 intergenic variant T/A;C snv 2
rs182381821 3 113643002 intergenic variant T/C snv 3.1E-03 2
rs28721484
PXYLP1 ; ZBTB38
3 141334437 intron variant C/T snv 0.22 2
rs397778224 16 19912366 regulatory region variant -/C delins 0.21 2
rs4477562 13 53530833 intron variant C/T snv 0.12 2
rs494558
COL4A1
13 110276815 intron variant C/T snv 0.90 2
rs577358806
LINC01822
2 21691067 intron variant C/T snv 1.5E-03 2
rs58231626
PAX8 ; PAX8-AS1
2 113256632 non coding transcript exon variant G/A snv 6.8E-04 2
rs6587515 1 150636412 regulatory region variant G/A snv 7.2E-02 2
rs6864091
POC5
5 75714177 intron variant T/C snv 0.43 2
rs6943127
CALCR
7 93568946 intron variant T/G snv 0.29 2
rs7187961
FTO
16 53792122 intron variant T/C snv 0.86 2
rs761567588
CDYL
6 4790301 intron variant A/G snv 1.3E-04 2
rs7777593 7 36506461 downstream gene variant T/A;G snv 2
rs8062405
ATXN2L
16 28826585 non coding transcript exon variant A/G snv 0.35 2