Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11667509
MARK4 ; EXOC3L2 ; BLOC1S3
19 45212934 3 prime UTR variant G/C snv 0.28 1
rs116685461
HLA-B
6 31347735 intron variant G/A snv 0.14 1
rs11671005
ZNF324B
19 58452163 5 prime UTR variant G/A snv 0.22 1
rs11696739
SIRPB1
20 1620279 upstream gene variant G/A snv 0.34 1
rs117107187
ITGB3
17 47252031 upstream gene variant A/G snv 5.5E-03 1
rs1172129
TMCC2
1 205275844 intron variant T/A snv 0.30 1
rs1172130
TMCC2
1 205275825 intron variant G/A snv 0.30 1
rs11731274 4 6889728 intergenic variant T/A;G snv 2
rs11731606
PDLIM5
4 94534108 intron variant C/T snv 0.24 1
rs11734132 4 6889792 intergenic variant G/C snv 0.17 3
rs11764390
CD36
7 80586889 intron variant G/A snv 0.48 1
rs117672662
ACTN1
14 68958750 intron variant T/C snv 7.4E-03 3
rs11771053
ELMO1
7 37412510 intron variant G/T snv 0.17 1
rs118033845 10 11794093 TF binding site variant G/A snv 2.6E-02 1
rs11868206
AP2B1
17 35632228 intron variant G/A snv 0.23 1
rs11893307 2 190863318 regulatory region variant G/A snv 0.21 1
rs11920280
KALRN
3 124618265 intron variant A/G;T snv 1
rs11950562
MIR3936HG ; SLC22A4
5 132316836 intron variant A/C snv 0.37 1
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 3
rs12065624
C4BPA
1 207107394 intron variant A/T snv 0.10 1
rs12096438
LDLRAP1
1 25562931 non coding transcript exon variant C/A;T snv 2
rs12102677
CBFA2T3 ; LOC100129697
16 88950086 intron variant A/C snv 0.34 1
rs12155039
H2AZ2
7 44833526 intron variant C/A;T snv 2
rs12191082
ADGRF5
6 46918107 intron variant G/A snv 0.13 2
rs12271225
TRIM5
11 5669314 intron variant A/G;T snv 0.17 1