Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80278614 1 118869694 intergenic variant G/A;T snv 1
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs11893688
ADAM17
2 9555153 intron variant C/T snv 0.64 2
rs10181515
LOC646736
2 226154745 TF binding site variant C/T snv 0.26 1
rs10495563
ADAM17
2 9522081 3 prime UTR variant G/A;C;T snv 1
rs11680809 2 112813232 downstream gene variant C/A snv 0.55 1
rs1179494
FEZ2
2 36582353 intron variant G/A;C snv 1
rs12104672
LIMS1 ; GCC2-AS1
2 108534717 intron variant T/G snv 0.40 1
rs12623454 2 120568721 intergenic variant G/C;T snv 1
rs1374204
LOC101926974 ; LOC105374581
2 46257066 non coding transcript exon variant C/T snv 0.66 1
rs139557015
LINC01934
2 181207599 intron variant T/C snv 2.1E-02 1
rs17034876
LOC101926974 ; LOC105374581
2 46257171 non coding transcript exon variant C/T snv 0.68 1
rs186606513
CNNM3
2 96816264 5 prime UTR variant G/A;C;T snv 2.2E-02; 4.6E-05; 1.4E-04 1
rs2280235
STAT1
1.000 0.080 2 190979104 splice region variant A/G snv 0.23 1
rs2551347
ATAD2B ; KLHL29
2 23689531 non coding transcript exon variant C/T snv 0.68 1
rs4952673 2 43196731 intergenic variant G/A;C snv 1
rs4953353
EPAS1
2 46340137 intron variant G/A;C;T snv 1
rs56188432
ACVR1C
2 157550353 missense variant A/G;T snv 7.6E-04; 4.0E-06 1
rs754868
LOC112268413
2 42958392 intergenic variant A/G snv 0.53 1
rs7563664
CYTIP ; LOC105373712
2 157487943 5 prime UTR variant G/T snv 0.20 1
rs7575873
ATAD2B
2 23739777 intergenic variant A/G snv 1.0E-01 1
rs7596521 2 46691526 regulatory region variant A/G snv 0.31 1
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 5