Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9521678
COL4A1
1.000 0.040 13 110263771 intron variant T/C snv 0.26 1
rs4773141
COL4A1
1.000 0.040 13 110302006 intron variant C/G snv 0.41 1
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 1
rs11838776
COL4A2
1.000 0.040 13 110388334 intron variant G/A snv 0.26 1
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs9515203
COL4A2
1.000 0.040 13 110397276 intron variant T/C snv 0.26 1
rs73562014
LINC02732
1.000 0.040 11 110401537 intron variant G/A snv 0.17 1
rs111245230
SVEP1
1.000 0.040 9 110407495 missense variant T/C snv 2.6E-02 2.3E-02 3
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs9583531 1.000 0.040 13 110732814 intergenic variant T/G snv 0.19 1
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs56125973
SMARCA4
1.000 0.040 19 11077488 intron variant T/C snv 0.13 1
rs56289821
SMARCA4
1.000 0.040 19 11077571 intron variant G/A snv 0.10 1
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 2
rs2738447
LDLR
1.000 0.040 19 11116804 intron variant A/C snv 0.65 1
rs688
LDLR
0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 2
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 5
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 4
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3