Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7713917 0.925 0.040 5 79533426 upstream gene variant A/G snv 0.54 3
rs2640909
PER3
1 7830057 missense variant T/C snv 0.14 0.23 4
rs228682
PER3
1 7796286 intron variant T/C snv 0.35 2
rs3936093
LINGO1
1.000 0.040 15 77809567 intron variant A/G snv 0.47 2
rs7175083
LINGO1
1.000 0.040 15 77714500 intron variant T/C snv 0.50 2
rs73425402
NAV3
0.925 0.040 12 77503518 intron variant T/A snv 4.1E-02 3
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs12137398
CAMTA1
1.000 0.040 1 7730488 intron variant C/T snv 0.14 2
rs116362708
SLC44A5
1.000 0.040 1 75464629 intron variant G/A snv 2.3E-02 2
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs10144845
YLPM1
1.000 0.040 14 74771067 intron variant C/T snv 0.62 2
rs8004430
AREL1
1.000 0.040 14 74704980 intron variant C/T snv 0.72 2
rs6782011
GRM7
0.807 0.120 3 7457960 intron variant C/T snv 0.52 7
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs9930139
RBFOX1
1.000 0.040 16 7239569 intron variant A/C;T snv 2
rs12137936
NEGR1
1.000 0.040 1 72254674 intron variant C/G snv 0.23 2
rs571720664
DLG4
17 7203556 missense variant C/G;T snv 4.0E-06 2
rs4131347 12 71930591 downstream gene variant G/A;C snv 1
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs4902704
EXD2 ; LOC105370550
1.000 0.040 14 69236871 intron variant G/C snv 0.72 2
rs77607745 1.000 0.040 13 69001052 intergenic variant A/C snv 0.15 2
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106