Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 4
rs34720381
PRRC2C
1 171486183 intron variant C/T snv 7.3E-02 4
rs545608
CRYZL2P-SEC16B ; SEC16B
0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 3
rs10923724 1 119004219 upstream gene variant C/T snv 0.53 3
rs11209951
LOC105378797
1 72371807 intron variant C/T snv 0.61 3
rs113722913
LOC105371682
1 199950846 intergenic variant T/C snv 2.6E-02 3
rs12128108
AGBL4
0.925 0.040 1 49827749 intron variant C/G;T snv 3
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs2785980
LYPLAL1-AS1
1 219527177 intergenic variant T/C snv 0.28 3
rs2820292
NAV1 ; IPO9-AS1
1 201815159 intron variant A/C snv 0.48 3
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 3
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 3