Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 3
rs10143078
COX16 ; SYNJ2BP-COX16 ; SYNJ2BP
14 70414772 intron variant A/C snv 6.6E-02 1
rs10197121
RRM2
2 10153562 intron variant C/T snv 0.64 1
rs10444602 12 131708291 upstream gene variant T/G snv 0.51 1
rs10555137
CASC8
8 127457345 intron variant C/T snv 6.6E-02 1
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 5
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 3
rs11105354
ATP2B1
12 89632746 intron variant A/G snv 0.15 1
rs11160059
SLC24A4
14 92340986 intron variant T/A;C snv 1
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 3
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 1
rs11222084
ZBTB44-DT
11 130403335 non coding transcript exon variant A/T snv 0.30 1
rs1156725
SOX6
11 16286154 intron variant C/T snv 0.78 1
rs11659639 18 60500379 intron variant T/G snv 1.1E-02 1
rs1173756
NPR3
5 32789746 3 prime UTR variant T/C snv 0.56 0.60 1
rs1173766 5 32804422 intergenic variant T/C snv 0.57 1
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 4
rs11816631 10 97802815 intergenic variant A/G snv 8.8E-02 1
rs11823543
ZPR1
11 116778419 3 prime UTR variant G/A snv 0.11 2
rs11825181
BUD13
11 116755542 intron variant G/A snv 0.10 1
rs12067906 1 192462868 intron variant T/C snv 0.12 1
rs12098903 11 55899037 downstream gene variant A/T snv 5.7E-02 1
rs12098904 11 55899077 downstream gene variant A/T snv 5.7E-02 1
rs12098941 11 55898967 downstream gene variant T/A;G snv 1