Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6904416 6 98542613 regulatory region variant T/C snv 0.12 1
rs12813389
USP44
12 95519786 intron variant A/T snv 0.64 1
rs11108056 12 95461609 regulatory region variant C/G;T snv 1
rs112635299
SERPINA2
1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 7
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 4
rs4841133
LOC157273
8 9326154 non coding transcript exon variant A/G snv 0.87 2
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs7012637 8 9315699 intron variant G/A;C snv 3
rs1408282 6 93142534 intergenic variant G/A snv 9.6E-02 1
rs17519972
GLMN ; RPAP2
1.000 0.080 1 92362948 intron variant A/C snv 0.15 2
rs469882 1 91064875 intergenic variant A/C;T snv 1
rs469772 1 91064748 intergenic variant C/T snv 0.19 2
rs1332328
LIPA
10 89251701 intron variant C/T snv 0.38 1
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 1
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 2
rs4246598
LOC101928347
2 88138531 intergenic variant C/A snv 0.44 1
rs1998303 9 82800066 intergenic variant A/G snv 0.37 2
rs4703642
LOC105379040
5 74966337 intron variant A/G snv 0.50 3
rs7795281
LOC101926943 ; GTF2I
7 74708523 intron variant G/A snv 0.79 1
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 2
rs2384955
CD300LF ; RAB37
17 74699028 intron variant T/C snv 0.69 1
rs111269058 7 73561372 upstream gene variant C/T snv 9.8E-02 1
rs13233571
BCL7B
0.925 0.120 7 73556901 intron variant C/T snv 9.2E-02 2
rs13244268
BAZ1B
0.925 0.120 7 73497513 intron variant T/C snv 9.2E-02 2