Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7948458
IGF2 ; INS-IGF2
11 2151600 intron variant A/C snv 0.76 1
rs151204774 11 21580341 downstream gene variant AATT/- delins 7.4E-02 1
rs577358806
LINC01822
2 21691067 intron variant C/T snv 1.5E-03 2
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs16877106
ANAPC4
4 25401644 intron variant C/T snv 4.9E-02 1
rs1840440 18 25677222 intergenic variant T/C;G snv 1
rs965178 18 25681256 intergenic variant T/C snv 0.53 1
rs4145878
H3C4 ; H2BC7
6 26197818 intron variant T/A snv 0.58 1
rs7336332 13 27484267 upstream gene variant A/G snv 0.19 1
rs6416056
BDNF-AS ; LINC00678
11 27625198 intron variant G/A snv 0.71 1
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs11030102
BDNF ; BDNF-AS
11 27660049 non coding transcript exon variant C/G snv 0.19 2
rs8062405
ATXN2L
16 28826585 non coding transcript exon variant A/G snv 0.35 2
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 9
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 5
rs3132479
LOC112267902 ; HLA-B
6 31306975 intron variant A/C;G snv 1
rs2256174
MICA
6 31412645 intron variant A/G snv 0.64 1
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 5
rs12625495
ZNF341
20 33775731 intron variant G/A;C;T snv 2
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 6
rs7261964
PIGU
20 34617207 intron variant C/T snv 0.85 1
rs112540634
ILRUN
6 34656128 intron variant C/G;T snv 2
rs116975424
RFX3
9 3518833 intron variant T/C snv 2.6E-02 2
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17