Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs28583049
LOC105374033
0.882 3 108724568 downstream gene variant T/C snv 0.17 4
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs57791671 0.882 3 121889586 upstream gene variant T/A snv 0.38 4
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs5865
TMEM131
0.851 0.040 2 97756543 3 prime UTR variant C/T snv 0.62 5
rs1800601
NTRK1 ; SH2D2A
0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 4
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14