Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 8
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 5
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 4
rs34720381
PRRC2C
1 171486183 intron variant C/T snv 7.3E-02 4
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 3
rs1890995
TGFB2
1 218431336 intron variant G/A snv 0.33 3
rs28673728
INPP5B ; LOC105378651
1 37943401 intron variant A/G snv 0.40 3
rs3795503
LOC107985231 ; KIAA1614
1 180936558 synonymous variant C/T snv 0.31 0.27 3
rs9435733
MFAP2
1 16981759 intron variant T/C snv 0.41 3
rs1044299
PAPPA2
1 176842737 3 prime UTR variant C/G;T snv 2
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 2
rs10482795
TGFB2
1 218432267 intron variant G/A;T snv 2
rs12408663
NBL1 ; MICOS10-NBL1
1 19641564 intron variant T/C snv 0.19 2
rs141942982 1 155164919 downstream gene variant G/A;T snv 2
rs1472565
CAPZB
1 19428536 intron variant T/A;C snv 2
rs17393468 1 9378481 intergenic variant T/C snv 0.14 2
rs187799739
RPRD2
1 150452900 intron variant C/A;G snv 2
rs1926872 1 184049341 upstream gene variant T/C snv 0.29 2
rs2061708
COL11A1
1 102951647 intron variant G/A;C;T snv 2
rs212526
ECE1
1 21258448 intron variant T/C snv 0.68 2
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 2