Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs11210892 1.000 0.040 1 43634413 intergenic variant G/A snv 0.51 3
rs1620977
NEGR1
1.000 0.040 1 72263459 intron variant A/G;T snv 3
rs2391769
LOC105378866
0.925 0.040 1 96513405 regulatory region variant A/G;T snv 3
rs11210195
LOC105378800
1.000 0.040 1 73283600 intergenic variant C/T snv 0.44 2
rs1498232 1.000 0.040 1 29961104 regulatory region variant T/C snv 0.53 2
rs17659437 1.000 0.040 1 177337251 intergenic variant T/C snv 0.13 2
rs1782810
MIR137HG
1.000 0.040 1 98036784 intron variant G/A;T snv 2
rs301798
RERE ; RERE-AS1
1.000 0.040 1 8428505 non coding transcript exon variant A/G snv 0.30 2
rs35998080
LINC02797
1.000 0.040 1 72812932 intron variant G/T snv 0.37 2
rs61789073
LINC01930 ; MIR137HG ; DPYD
1.000 0.040 1 97938540 intron variant T/C snv 4.9E-02 2
rs7521492 1.000 0.040 1 163758686 intergenic variant A/G snv 0.60 2
rs11185408 1 104249635 intergenic variant G/A;C snv 0.55 1
rs201910565 1 96096246 regulatory region variant T/-;TT;TTT delins 1
rs6692705 1 193533479 intron variant A/C;G snv 1
rs6701243 1 98627228 intergenic variant A/C snv 0.37 1
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs11682175
ACTG1P22
0.925 0.040 2 57760458 intron variant T/C snv 0.38 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 3
rs10211550
MOB4 ; HSPE1-MOB4
1.000 0.040 2 197518575 intron variant G/T snv 0.37 2