Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 3
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs3934834
LOC105378948 ; LOC112267874
1 1070426 downstream gene variant C/T snv 0.21 2
rs6027281
LOC107985429
20 60081096 downstream gene variant T/C snv 0.31 2
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 4
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs12964056 18 60006567 upstream gene variant A/G;T snv 2
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs7001819
LOC105379243
0.925 0.080 8 11792966 upstream gene variant T/C snv 0.35 2
rs7359397
SH2B1
1.000 0.040 16 28874338 upstream gene variant C/T snv 0.28 2
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 3
rs1561288
EFR3B
2 25146133 3 prime UTR variant C/T snv 0.29 2
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 2
rs2253802
MDC1
6 30716909 5 prime UTR variant C/T snv 4.4E-02 2
rs2272903
TFAP2B
6 50818858 5 prime UTR variant G/A;C snv 0.15 2
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 2
rs11951673
LOC101929710 ; CAST
5 96525308 non coding transcript exon variant C/T snv 0.39 2
rs2440238
PAX6-AS1 ; PAUPAR
11 31886440 non coding transcript exon variant T/G snv 0.32 2
rs3764400
NFE2L1 ; COPZ2
17 48046570 non coding transcript exon variant T/C snv 0.11 2
rs623312
PAUPAR ; PAX6-AS1
11 31885918 non coding transcript exon variant G/A snv 0.32 2