Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs2922763 8 75661476 intergenic variant G/T snv 0.77 2
rs1167800
HIP1
7 75546898 intron variant A/G snv 0.34 2
rs4704220
CERT1
5 75461731 intron variant G/A snv 0.55 5
rs113313252
TNNI3K ; FPGT-TNNI3K ; LRRC53
1 74534327 intron variant -/T delins 2
rs12142020
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1 74534327 intron variant A/T snv 0.50 2
rs201167096
FPGT-TNNI3K ; LRRC53 ; TNNI3K
1 74534327 intron variant -/T delins 2
rs1514175
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1.000 0.080 1 74525960 intron variant A/G snv 0.48 2
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 2
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 2
rs4776970
MAP2K5
15 67788548 intron variant A/T snv 0.44 2
rs997295
MAP2K5 ; LOC107984718
1.000 0.040 15 67724005 intron variant G/A;T snv 2
rs10188334 2 653874 regulatory region variant C/A;T snv 0.15 2
rs13397165 2 653354 intergenic variant G/A snv 0.18 2
rs13396935 2 653195 intergenic variant G/A snv 0.18 2
rs13415094 2 653093 intergenic variant T/C snv 0.19 2
rs7574359 2 652542 intergenic variant T/C;G snv 2
rs7608050 2 652247 regulatory region variant G/A;T snv 2
rs6719980 2 651507 intergenic variant T/C snv 0.19 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs12714414 2 651407 intergenic variant T/C snv 0.18 2
rs2867113 2 651365 intergenic variant G/A snv 0.18 2