Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10058621 5 51259335 intergenic variant T/C snv 6.0E-02 1
rs11074779 16 26440122 intergenic variant T/C snv 0.16 1
rs11177782
LOC105369823 ; BEST3
12 69662005 intron variant C/T snv 1.2E-02 1
rs111882035
ARHGAP24
4 85495401 intron variant A/G snv 1.9E-02 1
rs112108866
CAPN12
19 38761240 intron variant C/A;G snv 1.7E-02 1
rs113338984
SNTB2
16 69282015 intron variant C/A;T snv 1
rs116330320
LINC01060
4 188507189 intron variant G/A;T snv 3.6E-02 1
rs117609474
LINC02331
14 53804550 intron variant A/G snv 1.0E-02 1
rs11775026
C8orf89
8 73264813 intergenic variant T/C snv 5.9E-02 1
rs118130881
LOC101929492
8 31371254 intron variant A/G snv 1
rs12268753
PRKG1
10 52058389 intron variant A/C;T snv 1
rs12295181
HBG2 ; HBE1
11 5270506 intron variant C/T snv 0.11 1
rs12436690 14 97119552 intron variant G/A snv 0.12 1
rs12990252 2 35861457 intergenic variant G/C snv 0.18 1
rs13053731
MIR6819 ; MYH9
22 36286661 intron variant G/A snv 5.7E-02 1
rs13166268 5 121024223 intergenic variant C/G snv 9.2E-02 1
rs13360092
LOC107986379
5 51233341 intergenic variant G/A snv 6.0E-02 1
rs139139710
GALNT17
7 71678504 intron variant C/A snv 2.7E-02 1
rs140454225 16 1003856 upstream gene variant T/C;G snv 1
rs142614863
ERBIN
5 65950288 intron variant C/T snv 1.2E-02 1
rs143985312
LRRTM4
2 77072001 intron variant T/C snv 9.4E-03 1
rs1449587 13 48839332 regulatory region variant C/T snv 0.31 1
rs145471199 7 9407441 intergenic variant A/G;T snv 1
rs147828834
FSIP1
15 39602982 intron variant A/T snv 8.3E-03 1
rs148410317
IFITM10
11 1749985 intron variant G/A;C snv 1