Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs3755967
GC
0.925 0.080 4 71743681 intron variant C/A;T snv 6
rs12800438
NADSYN1
1.000 0.080 11 71459957 non coding transcript exon variant G/A;T snv 5
rs1155563
GC
0.925 0.080 4 71777771 intron variant T/A;C snv 4
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 3
rs2302190
MTMR4
17 58507147 missense variant T/A;C snv 0.24 3
rs4944062
NADSYN1
11 71476248 3 prime UTR variant G/A;T snv 2
rs55665837
COPB1
11 14473503 intron variant C/G;T snv 2
rs6730714 2 222184302 intergenic variant G/A;T snv 2
rs8018720
SEC23A
14 39086981 missense variant G/C;T snv 0.80; 1.1E-04 2
rs843005
GC
4 71750610 intron variant C/A;T snv 2
rs182244780
RRAS2
11 14363985 intron variant G/A snv 6.0E-03 2
rs117865811
SPON1
11 14180763 intron variant A/G snv 6.3E-03 2
rs117300835 11 15097429 intergenic variant G/A snv 7.6E-03 2
rs117913124
CYP2R1
11 14879385 synonymous variant G/A snv 1.7E-02 1.6E-02 2
rs719700 12 45635426 intergenic variant T/C snv 1.8E-02 2
rs116970203
PDE3B
11 14855172 intron variant G/A snv 2.2E-02 2
rs79666294 5 155047146 regulatory region variant C/T snv 2.2E-02 2
rs12868495 13 34067425 intergenic variant G/A snv 2.3E-02 2
rs148189294 4 71575200 downstream gene variant G/A snv 2.6E-02 2
rs79761689 4 72005565 intergenic variant T/C snv 3.7E-02 2
rs78862524
ADAMTS3
4 72305473 intron variant C/A snv 3.9E-02 3
rs138485827 4 72166226 intergenic variant C/T snv 5.0E-02 2