Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 7
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs4691380
PDGFC
4 156798972 intron variant C/T snv 0.45 4
rs113722913
LOC105371682
1 199950846 intergenic variant T/C snv 2.6E-02 3
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 3
rs13273088
SULF1
8 69581739 intron variant G/A snv 0.81 3
rs2300835
AKAP6
14 32738316 intron variant C/A snv 0.16 3
rs2745353
RSPO3
6 127131790 intron variant C/T snv 0.55 3
rs2785980
LYPLAL1-AS1
1 219527177 intergenic variant T/C snv 0.28 3
rs308971
SYN2
3 12075120 intron variant G/A snv 0.82 3
rs35747
LOC105369944
12 102518780 intergenic variant G/A snv 0.70 3
rs4646949
TAF11 ; UHRF1BP1
6 34877672 3 prime UTR variant T/C;G snv 3
rs6689335
LYPLAL1-AS1
1 219455340 intron variant T/C snv 0.31 3
rs731839
PEPD
19 33408159 intron variant G/A snv 0.63 3
rs8182584
PEPD
19 33418804 intron variant T/C;G snv 3
rs912056
LOC101928004
6 6735964 intron variant A/T snv 0.66 3
rs9552416 13 18737101 downstream gene variant C/A;T snv 3
rs9841287
LOC107986040 ; LOC105376921
3 67310 intergenic variant A/G snv 0.22 3
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs11231693
MACROD1 ; FLRT1
11 64095140 intron variant G/A snv 0.11 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 2
rs4715210 6 50929538 regulatory region variant C/G;T snv 2
rs4776970
MAP2K5
15 67788548 intron variant A/T snv 0.44 2