Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10988944
ERP44
0.925 0.040 9 100011933 intron variant C/A snv 0.20 2
rs6745099
AFF3
0.925 0.040 2 100122979 intron variant C/G snv 0.13 2
rs7960152 0.925 0.040 12 100181995 intron variant A/C snv 0.84 2
rs35768 0.925 0.040 12 100191661 intron variant T/C snv 0.12 2
rs3737
DEPDC4 ; ACTR6
0.925 0.040 12 100224284 3 prime UTR variant C/G snv 6.3E-02 2
rs9291
YY1 ; SLC25A29
0.925 0.040 14 100282507 3 prime UTR variant A/C snv 0.89 2
rs7150701
WARS1
0.925 0.040 14 100363922 intron variant C/G;T snv 2
rs17095079 0.925 0.040 11 100473473 intergenic variant T/C snv 3.8E-02 2
rs7074041 0.925 0.040 10 100578375 intergenic variant A/G;T snv 7.6E-02 2
rs10760734 0.925 0.040 9 100621917 intergenic variant G/C snv 0.84 2
rs1283198
TMTC4
0.925 0.040 13 100672046 intron variant C/T snv 0.60 2
rs2138050
ANO4
0.925 0.040 12 100886729 intron variant C/G;T snv 0.33 2
rs17654410
ARHGAP42
0.925 0.040 11 100993415 3 prime UTR variant C/T snv 9.3E-02 2
rs621332
NALCN
0.925 0.040 13 101081066 intron variant C/A snv 0.36 2
rs4906048 0.925 0.040 14 101118665 upstream gene variant T/C snv 0.90 2
rs11190870 0.827 0.200 10 101219450 intergenic variant T/A;C snv 3
rs678741
LBX1-AS1
0.851 0.200 10 101237824 intron variant G/A snv 0.51 2
rs2762662 0.925 0.040 10 10127867 intergenic variant G/A snv 5.5E-02 2
rs3016235 0.925 0.040 11 101402145 intergenic variant G/C snv 0.86 2
rs4965897 0.925 0.040 15 101545397 intergenic variant G/A snv 0.54 2
rs17031683
LOC105369938 ; MYBPC1
0.925 0.040 12 101611608 intron variant A/C snv 6.0E-02 2
rs1114783
LOC105379102
0.925 0.040 5 101837083 intergenic variant G/A snv 0.97 2
rs1046774
ZMAT1
0.925 0.040 X 101882824 3 prime UTR variant G/A;T snv 2
rs4337094
DRAM1
0.925 0.040 12 101948325 intron variant G/A snv 0.29 2
rs9838540
ZPLD1
0.925 0.040 3 102267159 intron variant A/C snv 0.49 2