Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646179
USP1
1 62437203 5 prime UTR variant A/G;T snv 2
rs6540555
TRAF3IP3
1 209763226 intron variant A/G snv 0.36 2
rs72660908
RSRP1
1 25257119 intron variant C/G snv 0.26 2
rs78024727 1 198580649 intergenic variant G/A snv 3.5E-02 2
rs826415
TENT5C
1 117611355 intron variant T/G snv 0.27 2
rs10495161 1 220963330 regulatory region variant C/T snv 0.14 1
rs1078859
LYST
1 235748725 intron variant C/A snv 0.26 1
rs10801682
PKN2
1 88708570 intron variant A/T snv 0.50 1
rs1085244
P3R3URF-PIK3R3 ; PIK3R3
1 46098008 intron variant C/A snv 0.45 1
rs11119256
DYRK3
1 206660258 intron variant C/G snv 0.54 1
rs11119337
TRAF3IP3
1 209760788 intron variant A/G snv 0.42 1
rs115159272
SPAG17
1 118125195 intron variant T/C;G snv 1
rs116135446
RGS7
1 240794633 intron variant C/T snv 2.6E-02 1
rs1172135
TMCC2
1 205278032 non coding transcript exon variant G/C;T snv 1
rs11807602 1 93073392 intergenic variant C/G snv 0.32 1
rs12022684
TIE1
1 43304847 splice region variant C/G snv 3.4E-02 1.4E-02 1
rs12026918 1 65680563 intergenic variant C/G snv 0.29 1
rs12033311 1 117644577 upstream gene variant C/T snv 4.1E-02 1
rs12037805
SLC6A9 ; LOC107984948
1 44031577 intron variant T/C snv 0.25 1
rs12127002 1 39919296 regulatory region variant G/A snv 9.4E-02 1
rs12128213 1 200228410 intergenic variant A/G snv 0.35 1
rs12130660
NUP210L
1 154115782 intron variant T/C snv 3.3E-02 1
rs12740790
RPA2
1 27916023 upstream gene variant A/G snv 0.60 1
rs143683645 1 117788172 intergenic variant C/G;T snv 1
rs165316 1 91067740 intergenic variant A/G snv 0.19 1