Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 4
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs2820436
LYPLAL1-AS1
0.882 0.040 1 219467338 intergenic variant A/C;G snv 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs10429950 1.000 0.040 1 218451191 intergenic variant T/C snv 0.33 3
rs10923724 1 119004219 upstream gene variant C/T snv 0.53 3
rs11209951
LOC105378797
1 72371807 intron variant C/T snv 0.61 3
rs12731372 1 118310352 regulatory region variant C/T snv 0.19 3
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 3
rs7550711
GPR61
1 109540264 intron variant C/T snv 2.6E-02 3
rs984222
TBX15
1 118961220 intron variant C/A;G snv 3
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
rs12406019 1 78212446 intergenic variant A/G snv 0.32 2
rs1707322 1 46039475 downstream gene variant A/G snv 0.68 2