Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1145652 5 165337081 intergenic variant A/G snv 9.6E-02 1
rs11662721
ABHD3
18 21681452 intron variant C/T snv 0.15 1
rs11667159 19 46291989 intergenic variant C/A;T snv 3
rs11668290 19 46292921 upstream gene variant G/A snv 0.12 3
rs11671319 19 46291810 intergenic variant T/C snv 0.12 3
rs11671360 19 46291914 intergenic variant T/C snv 0.12 3
rs11671710 19 46288677 regulatory region variant C/G;T snv 3
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs11730235
STIM2
4 26922822 intron variant G/T snv 0.26 1
rs117366905 19 46294033 upstream gene variant A/G snv 0.12 3
rs117992292 19 46294038 upstream gene variant A/G snv 0.12 3
rs12098564
LINC01519
10 85193571 non coding transcript exon variant A/G snv 7.4E-02 2
rs12190237
SYCP2L
6 10922405 intron variant G/A snv 0.24 1
rs12195587
ELOVL2
6 10989709 synonymous variant G/A snv 0.12 0.11 1
rs12199131
LOC101928191 ; SYCP2L
6 10932336 intron variant G/A;T snv 1
rs12200867
SYCP2L ; LOC101928191
6 10939591 intron variant C/G snv 0.22 1
rs12207488
LOC101928191 ; SYCP2L
6 10952103 intron variant G/A snv 0.19 1
rs12213249
SYCP2L
6 10926709 intron variant C/T snv 0.19 1
rs12214825
LOC101928191 ; SYCP2L
6 10933145 intron variant C/T snv 0.20 1
rs1225717
SYCP2L
6 10978007 intron variant A/G;T snv 1
rs1225736
LOC101928191 ; SYCP2L
6 10939156 intron variant A/G snv 0.24 1
rs1225737
ELOVL2
6 10982419 3 prime UTR variant C/T snv 0.59 1
rs1225741
SYCP2L ; LOC101928191
6 10952010 intron variant G/A snv 0.39 1
rs1225744
LOC101928191 ; SYCP2L
6 10954307 intron variant C/T snv 0.35 1
rs1225753
SYCP2L
6 10956456 intron variant G/A snv 0.43 1