Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11338281
SLC2A9
4 9959218 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 1
rs1332101 10 99545585 intergenic variant G/A snv 0.25 2
rs12412214 10 99516499 intergenic variant G/A snv 0.26 1
rs139472942
TRRAP
7 98928934 intron variant C/T snv 1.4E-02 1
rs7019033 9 98030894 upstream gene variant G/A snv 0.25 1
rs472109
SWAP70
1.000 0.040 11 9748771 intron variant G/C;T snv 2
rs35362007
GLRX5 ; SNHG10
14 95536861 intron variant G/A snv 0.27 3
rs496321
LOC101929295
11 95153468 intron variant T/C;G snv 3
rs59883166
LOC643339
12 93364543 intron variant T/-;TT;TTT delins 2
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs17700466 7 93006659 regulatory region variant A/C snv 0.12 2
rs10225965
LOC112268009 ; CDK6
7 92644264 intron variant C/T snv 0.26 1
rs2040494
CDK6
7 92627591 intron variant C/T snv 0.64 2
rs206913
BACH2
6 90227175 intron variant C/A snv 0.70 1
rs1964356
LOC105379227 ; ERI1
8 8995760 regulatory region variant G/T snv 0.34 1
rs9931440 16 89706016 upstream gene variant A/C;G snv 1
rs2239296
NPRL3
16 89369 non coding transcript exon variant G/A;C snv 1
rs62045844 16 89018519 intergenic variant C/T snv 3.2E-02 2
rs2067663
MEF2C ; MEF2C-AS1
5 88895818 intron variant C/T snv 0.22 3
rs861400 16 88795935 intergenic variant C/A;G snv 1
rs837763
LOC107984842
16 88787321 upstream gene variant C/G;T snv 4
rs4238686
PIEZO1
16 88722526 non coding transcript exon variant A/C;G snv 2
rs12232375
ZFPM1
16 88500003 intron variant G/A;C;T snv 2
rs6538148 12 88424702 intergenic variant C/G;T snv 3
rs68149176
SLC7A5 ; MIR11401
16 87852884 intron variant C/G;T snv 2