Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs551544003
SH3RF1
4 169152874 intron variant G/A snv 2.9E-04 1
rs58231626
PAX8 ; PAX8-AS1
2 113256632 non coding transcript exon variant G/A snv 6.8E-04 2
rs577358806
LINC01822
2 21691067 intron variant C/T snv 1.5E-03 2
rs182381821 3 113643002 intergenic variant T/C snv 3.1E-03 2
rs534356339
CCSER1
4 91335712 intron variant GAT/- del 3.4E-03 1
rs182624399 11 70019090 intron variant C/T snv 8.9E-03 1
rs116975424
RFX3
9 3518833 intron variant T/C snv 2.6E-02 2
rs80116344 18 60281167 intergenic variant G/A snv 3.9E-02 1
rs16877106
ANAPC4
4 25401644 intron variant C/T snv 4.9E-02 1
rs112037309
ARHGEF38 ; INTS12
4 105695979 intron variant G/A snv 6.7E-02 1
rs6587515 1 150636412 regulatory region variant G/A snv 7.2E-02 2
rs11863065 16 82293200 intergenic variant G/A snv 7.3E-02 3
rs151204774 11 21580341 downstream gene variant AATT/- delins 7.4E-02 1
rs72989246 18 60053966 TF binding site variant C/T snv 8.1E-02 1
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs12517906 5 180743819 upstream gene variant C/A;T snv 0.11 1
rs4477562 13 53530833 intron variant C/T snv 0.12 2
rs9313296 5 165950694 intergenic variant G/C snv 0.13 1
rs13029479 2 655222 regulatory region variant G/A snv 0.13 1
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs9813495
CADM2
3 85777231 intron variant A/G snv 0.15 4
rs11030102
BDNF ; BDNF-AS
11 27660049 non coding transcript exon variant C/G snv 0.19 2
rs7336332 13 27484267 upstream gene variant A/G snv 0.19 1
rs17109221
NRXN3
14 79443776 intron variant C/T snv 0.21 1