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
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs17216707 20 54115823 intergenic variant T/C snv 0.17 6
rs3755967
GC
0.925 0.080 4 71743681 intron variant C/A;T snv 6
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs11234027
NADSYN1
0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs12800438
NADSYN1
1.000 0.080 11 71459957 non coding transcript exon variant G/A;T snv 5
rs17467825 0.925 0.080 4 71739800 downstream gene variant A/G snv 0.22 4
rs1155563
GC
0.925 0.080 4 71777771 intron variant T/A;C snv 4
rs78862524
ADAMTS3
4 72305473 intron variant C/A snv 3.9E-02 3
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 3
rs2302190
MTMR4
17 58507147 missense variant T/A;C snv 0.24 3
rs11586313 1 152917994 TF binding site variant G/A;C snv 0.51 2
rs117300835 11 15097429 intergenic variant G/A snv 7.6E-03 2
rs12287212 11 14428315 intergenic variant C/A snv 0.31 2
rs12868495 13 34067425 intergenic variant G/A snv 2.3E-02 2
rs138485827 4 72166226 intergenic variant C/T snv 5.0E-02 2
rs1410656 13 46968386 intergenic variant T/C snv 0.97 2
rs148189294 4 71575200 downstream gene variant G/A snv 2.6E-02 2