Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 2
rs10018902 4 120941346 intergenic variant G/A;T snv 1
rs1056513
PATJ
1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 1
rs11863065 16 82293200 intergenic variant G/A snv 7.3E-02 1
rs12517906 5 180743819 upstream gene variant C/A;T snv 0.11 1
rs16877106
ANAPC4
4 25401644 intron variant C/T snv 4.9E-02 1
rs17668565 5 92818872 intergenic variant T/A;C snv 1
rs1840440 18 25677222 intergenic variant T/C;G snv 1
rs1973993 1 96478438 intergenic variant T/C snv 0.49 1
rs494558
COL4A1
13 110276815 intron variant C/T snv 0.90 1
rs7336332 13 27484267 upstream gene variant A/G snv 0.19 1
rs7624084
ZBTB38
3 141374443 intron variant T/C snv 0.54 1
rs7777593 7 36506461 downstream gene variant T/A;G snv 1
rs9313296 5 165950694 intergenic variant G/C snv 0.13 1
rs965178 18 25681256 intergenic variant T/C snv 0.53 1
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 3
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 3
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 1
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 4
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 4