Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 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
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 5
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5
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
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4