Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs1155563
GC
0.925 0.080 4 71777771 intron variant T/A;C snv 4
rs17467825 0.925 0.080 4 71739800 downstream gene variant A/G snv 0.22 4
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 3
rs78862524
ADAMTS3
4 72305473 intron variant C/A snv 3.9E-02 3
rs1007392
PDE3B
11 14753045 intron variant A/G snv 0.35 2
rs10745742
AMDHD1
12 95964751 intron variant C/T snv 0.48 2
rs11023332
PDE3B
11 14762564 intron variant G/C snv 0.35 2
rs11586313 1 152917994 TF binding site variant G/A;C snv 0.51 2
rs116970203
PDE3B
11 14855172 intron variant G/A snv 2.2E-02 2
rs117300835 11 15097429 intergenic variant G/A snv 7.6E-03 2
rs117865811
SPON1
11 14180763 intron variant A/G snv 6.3E-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
rs13107347
NPFFR2
4 72109031 intron variant T/C snv 0.32 2