Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 5
rs72959041
RSPO3
6 127133748 intron variant G/A snv 3.2E-02 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs1452075
CADPS
1.000 0.040 3 62495388 intron variant C/T snv 0.73 4