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
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
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
rs17467825 0.925 0.080 4 71739800 downstream gene variant A/G snv 0.22 4
rs1007392
PDE3B
11 14753045 intron variant A/G snv 0.35 2
rs117865811
SPON1
11 14180763 intron variant A/G snv 6.3E-03 2
rs1526692 4 71713007 intergenic variant A/G snv 0.41 2
rs185378533
FLJ42102
11 71422087 intron variant A/G snv 0.68 2
rs2277458
GEMIN2 ; LOC105370459
14 39114277 5 prime UTR variant A/G snv 0.80 0.83 2
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs78862524
ADAMTS3
4 72305473 intron variant C/A snv 3.9E-02 3
rs12287212 11 14428315 intergenic variant C/A snv 0.31 2
rs3755967
GC
0.925 0.080 4 71743681 intron variant C/A;T snv 6
rs843005
GC
4 71750610 intron variant C/A;T snv 2
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 3
rs55665837
COPB1
11 14473503 intron variant C/G;T snv 2
rs10745742
AMDHD1
12 95964751 intron variant C/T snv 0.48 2
rs138485827 4 72166226 intergenic variant C/T snv 5.0E-02 2
rs3819817
HAL
12 95984993 intron variant C/T snv 0.50 2
rs4423214
NADSYN1
11 71462208 intron variant C/T snv 0.58 2
rs79666294 5 155047146 regulatory region variant C/T snv 2.2E-02 2
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs11234027
NADSYN1
0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs116970203
PDE3B
11 14855172 intron variant G/A snv 2.2E-02 2