Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 2
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 2
rs4242384 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 2
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 2
rs10934853
EEFSEC
0.882 0.160 3 128319530 intron variant C/A snv 0.43 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 1
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 2
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17 2
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 4
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs11155133
LOC102723724
0.925 0.200 6 140848688 intron variant A/G snv 8.5E-02 2
rs4624820 0.851 0.240 5 142302223 regulatory region variant G/A snv 0.55 3
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 3
rs3757318
CCDC170
0.882 0.160 6 151592978 intron variant G/A snv 6.1E-02 1
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 4
rs3126085
FLG-AS1
0.851 0.280 1 152328341 intron variant G/A snv 0.29 1
rs651164
SLC22A1
0.882 0.160 6 160160342 downstream gene variant A/G snv 0.69 2
rs9364554
SLC22A3
0.882 0.160 6 160412632 intron variant C/T snv 0.21 2
rs6556756
LOC105377703 ; LINC02143
0.882 0.160 5 164462274 intron variant G/T snv 0.89 2
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 3
rs6774494
MECOM
0.882 0.160 3 169364845 intron variant G/A snv 0.42 1