Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24 9
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 5
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38 4
rs11078925
ZPBP2
0.925 0.160 17 39868955 intron variant T/C snv 0.36 3
rs11557466
ZPBP2
0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36 3
rs11870965
ZPBP2
0.925 0.160 17 39873952 intron variant T/A snv 0.40 3
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs1054609
ZPBP2
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 2
rs11655198
ZPBP2
1.000 0.080 17 39869916 intron variant C/T snv 0.43 1
rs10404342
ZNF71-SMIM17 ; ZNF71
1.000 0.080 19 56620870 intron variant C/A snv 0.17 1
rs112502960
ZNF652 ; LOC102724596
1.000 0.080 17 49361940 5 prime UTR variant G/A snv 0.28 1
rs12682865
ZNF618
1.000 0.080 9 113979934 intron variant T/C snv 0.27 1
rs4979311
ZNF618
1.000 0.080 9 113987250 intron variant G/C snv 0.27 1
rs2288884
ZNF614 ; LOC112268244
1.000 0.080 19 52029018 intron variant C/T snv 0.14 1
rs12460587
ZNF432 ; ZNF841
1.000 0.080 19 52083666 intron variant T/C;G snv 0.16 1
rs10995245
ZNF365 ; LOC105378327
0.882 0.160 10 62631615 intron variant G/A;C snv 3
rs114357009
ZNF311
1.000 0.080 6 28997735 intron variant G/A snv 3.2E-02 1
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs1460239
ZFPM2
1.000 0.080 8 104799137 intron variant C/T snv 0.49 1
rs12447718
ZFPM1
1.000 0.080 16 88503726 intron variant G/A snv 8.4E-02 1
rs2315646
ZBTB46
1.000 0.080 20 63748397 intron variant T/A;G snv 1
rs3741578
ZBTB39
1.000 0.080 12 57000851 3 prime UTR variant G/C snv 6.8E-02 1
rs7625643
ZBTB38
0.925 0.080 3 141431184 intron variant A/G snv 0.51 3
rs1672691
ZBTB16
1.000 0.080 11 114071429 intron variant C/T snv 0.19 1
rs11225138
YAP1
0.925 0.200 11 102123167 intron variant G/C snv 6.1E-02 2