Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs5934505 0.776 0.120 X 8945785 intergenic variant T/A;C snv 10
rs6152
AR
0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 9
rs2497938 0.807 0.080 X 67343176 intergenic variant T/C snv 0.37 7
rs6625163 0.807 0.080 X 67291142 intergenic variant G/A snv 0.62 7
rs7061504
OPHN1
0.807 0.080 X 68143959 intron variant A/G snv 0.23 7
rs12558842 0.925 0.080 X 67261958 intergenic variant C/A;G snv 2
rs3138869
AR
0.925 0.080 X 67546514 frameshift variant -/CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCG delins 2
rs5919427
LOC105373241
0.925 0.080 X 67783742 intergenic variant C/A snv 2
rs111810219
ARHGEF9
1.000 0.080 X 63717947 intron variant G/A snv 2.3E-02 1
rs112069404 1.000 0.080 X 66331306 intergenic variant C/A;T snv 1
rs113222435 1.000 0.080 X 67743865 intergenic variant G/T snv 2.5E-02 1
rs11796997
HAUS7 ; BGN
1.000 0.080 X 153494403 intron variant G/A snv 0.28 1
rs138216499 1.000 0.080 X 55304526 intergenic variant G/A snv 5.8E-02 1
rs138876904 1.000 0.080 X 65832298 intergenic variant C/T snv 8.3E-03 1
rs139470886
FAAH2
1.000 0.080 X 57282697 upstream gene variant G/A snv 4.3E-02 1
rs140488081
OPHN1
1.000 0.080 X 68276160 intron variant C/T snv 2.8E-02 1
rs140707533 1.000 0.080 X 54597955 regulatory region variant G/A snv 4.7E-02 1
rs140914450
MTND1P31
1.000 0.080 X 62842906 non coding transcript exon variant A/G snv 4.3E-02 1
rs142169094 1.000 0.080 X 67335270 intergenic variant A/G snv 0.13 1
rs143755874
MSN
1.000 0.080 X 65639521 intron variant G/A snv 2.1E-02 1
rs144393202 1.000 0.080 X 66894289 intergenic variant C/A;T snv 1
rs145867342 1.000 0.080 X 66322114 intergenic variant C/A;T snv 1
rs146112277 1.000 0.080 X 64535564 intergenic variant C/A snv 3.6E-02 1
rs146636673 1.000 0.080 X 67240489 intergenic variant G/C snv 1.5E-02 1