Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs5934505 0.776 0.120 X 8945785 intergenic variant T/A;C snv 10
rs34670419
ZKSCAN5
1.000 0.080 7 99533211 3 prime UTR variant G/A;T snv 7.7E-06; 2.6E-02 7
rs12150660
SHBG
1.000 0.040 17 7618597 intron variant G/T snv 0.17 5
rs6258
SHBG
1.000 0.040 17 7631360 missense variant C/A;T snv 5.6E-05; 4.5E-03 5
rs148982377
ZNF789 ; ZNF394
7 99477415 intron variant T/C snv 3.2E-02 4
rs72829446
ATP1B2
17 7648805 intron variant C/T snv 6.5E-02 3
rs2075230
MPDU1 ; LOC100996842
17 7583790 5 prime UTR variant A/C;G snv 4.0E-06; 0.19 3
rs1530530 13 24673148 regulatory region variant A/G;T snv 2
rs74585555 1.000 0.120 2 81214976 intergenic variant G/A snv 4.9E-02 2
rs4321386
IL1R2
2 101996551 intron variant C/G snv 0.12 2
rs10822184
REEP3
1.000 10 63577393 intron variant T/C;G snv 2
rs858516
SHBG
17 7633780 downstream gene variant C/G;T snv 2
rs4227
SOX15 ; MPDU1
1.000 0.120 17 7587859 3 prime UTR variant G/T snv 0.71 0.67 2
rs909814 1 22247449 intergenic variant T/C snv 0.59 1
rs35695070
FGF11
17 7440221 5 prime UTR variant CC/-;C;CCC;CCCC delins 1
rs35894069
POLR2A
17 7491857 intron variant G/A snv 0.24 1
rs9989479
POLR2A
17 7514792 downstream gene variant A/G;T snv 1
rs11078696
TNFSF12-TNFSF13 ; TNFSF12
17 7555982 intron variant G/T snv 0.60 1
rs62059803
TNFSF12-TNFSF13 ; TNFSF12
17 7548527 upstream gene variant C/T snv 0.15 1
rs34289079
WRAP53
17 7690001 intron variant T/C snv 0.21 1
rs3867595
ZBTB4
17 7476457 intron variant G/C snv 1.4E-02 1
rs67462449
ZBTB4
17 7474221 intron variant TTT/-;T;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT delins 1