Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs1558861 11 116736721 regulatory region variant C/G;T snv 3
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 3
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 2
rs7016880 8 20019235 intergenic variant G/C snv 8.5E-02 2
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 1
rs4635554 2 21166787 intergenic variant T/G snv 0.37 1
rs9644568 8 20071071 intergenic variant G/A snv 0.11 1
rs9949617
TMEM241
18 23299253 intron variant C/T snv 0.22 1
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 1
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs11634397 1.000 0.080 15 80139880 downstream gene variant A/G snv 0.57 1
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 1
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 1
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 1
rs972283
LOC105375508
1.000 0.080 7 130782095 intergenic variant A/G;T snv 1
rs11206517
PCSK9
1.000 0.120 1 55060755 intron variant T/C;G snv 2
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 2
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 2
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 1
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 1
rs46522
UBE2Z
0.807 0.120 17 48911235 non coding transcript exon variant C/T snv 0.40 1
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8