Source: ALL
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 9
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 5
rs2745353
RSPO3
6 127131790 intron variant C/T snv 0.55 5
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 5
rs4704220
CERT1
5 75461731 intron variant G/A snv 0.55 5
rs731839
PEPD
19 33408159 intron variant G/A snv 0.63 5
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 4
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 4
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs11231693
MACROD1 ; FLRT1
11 64095140 intron variant G/A snv 0.11 4
rs12714415 2 651430 intergenic variant T/C snv 0.19 4
rs4691380
PDGFC
4 156798972 intron variant C/T snv 0.45 4
rs4715210 6 50929538 regulatory region variant C/G;T snv 4
rs4776970
MAP2K5
15 67788548 intron variant A/T snv 0.44 4
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 4
rs10136789
KCNH5
14 62889535 intron variant T/C snv 0.15 3
rs10261878 7 25910925 intergenic variant A/C snv 0.80 3
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 3
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 3
rs1106683 7 131768766 intergenic variant G/A snv 0.14 3
rs113722913
LOC105371682
1 199950846 intergenic variant T/C snv 2.6E-02 3
rs1167800
HIP1
7 75546898 intron variant A/G snv 0.34 3
rs11951673
LOC101929710 ; CAST
5 96525308 non coding transcript exon variant C/T snv 0.39 3