Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 7
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 5
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 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
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5