Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs2820292
NAV1 ; IPO9-AS1
1 201815159 intron variant A/C snv 0.48 3
rs6437061
DIS3L2
2 232320342 intron variant A/C snv 0.56 3
rs12854631 X 58297412 intergenic variant A/C snv 2.7E-02 2
rs139214349 4 29168543 intron variant A/C snv 1.4E-02 2
rs147168872
SOS2
14 50173277 intron variant A/C snv 5.0E-03 2
rs1856293 6 133159801 intergenic variant A/C snv 0.56 2
rs72724928
LINGO2
9 28024196 intron variant A/C snv 3.3E-02 2
rs72923818
DYM
18 49157384 intron variant A/C snv 4.0E-02 2
rs1022261 4 35474678 intergenic variant A/C snv 0.52 1
rs12930834
ZFHX3
16 72917728 intron variant A/C snv 0.16 1
rs138045331
LOC105373592
2 122082314 intron variant A/C snv 3.9E-03 1
rs144528474
WDPCP
2 63650871 intron variant A/C snv 8.1E-04 1
rs6452791 5 88475276 intron variant A/C snv 0.55 1
rs12286929 0.925 0.080 11 115151684 intergenic variant A/C;G snv 4
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs4947642 7 51797912 intergenic variant A/C;G snv 3
rs6090583
EYA2
20 46930192 intron variant A/C;G snv 3
rs142383097
DFFA
1.000 0.040 1 10461101 3 prime UTR variant A/C;G snv 2.0E-02 2
rs189798510 17 14811500 intergenic variant A/C;G snv 2
rs2945731 8 133627845 intergenic variant A/C;G snv 4.9E-02 2
rs7897478 1.000 0.040 10 29945955 intergenic variant A/C;G snv 2
rs12022778
ELAVL4
1 50138323 intron variant A/C;G snv 0.21 1
rs1221976
DCC
18 52469766 intron variant A/C;G snv 1
rs2734971 6 29866672 intron variant A/C;G snv 1