Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9295733
SYCP2L
6 10965214 intron variant T/A;G snv 1
rs9295763
ELOVL2-AS1 ; ELOVL2
6 11044959 non coding transcript exon variant G/A;C;T snv 1
rs9368452
SYCP2L
6 10893446 intron variant G/C;T snv 1
rs9368564
ELOVL2-AS1
6 11060050 intron variant A/G;T snv 1
rs946350
SYCP2L
6 10892720 intron variant G/A;C snv 1
rs9467921
SYCP2L
6 10910386 intron variant C/G;T snv 1
rs953413
ELOVL2
6 11012626 intron variant G/A;C snv 1
rs9586180 13 103407783 intergenic variant T/C;G snv 1
rs9832727
LOC100507389
3 142930268 intron variant C/A;G;T snv 1
rs201922257
LIPG
18 49569492 missense variant C/T snv 1.7E-04 2.7E-04 2
rs541889526
MYO5B
18 50159516 intron variant A/T snv 1.0E-03 2
rs146524044
MYO5B
18 50057046 intron variant A/C snv 1.0E-03 2
rs535211063
MYO5B
18 50009408 intron variant A/G snv 1.0E-03 2
rs151159962
SKA1
18 50386938 intron variant T/C snv 1.3E-03 2
rs545804325
MYO5B
18 49940996 intron variant T/G snv 1.4E-03 2
rs538509310
SNHG22
18 49817040 intron variant T/A snv 1.7E-03 2
rs184392658
PIGT ; LOC105372631
20 45438925 intron variant T/C snv 3.0E-03 2
rs138572223 18 50446052 intergenic variant A/G snv 5.7E-03 2
rs139368489 18 50502045 intergenic variant T/C snv 5.8E-03 2
rs7102974
MIR611 ; FEN1 ; TMEM258
11 61792563 5 prime UTR variant C/T snv 8.5E-03 9.6E-03 1
rs12459897 19 31105872 intron variant G/T snv 1.2E-02 1
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs1514178
LOC101926964
1 60739797 intron variant T/C snv 1.5E-02 1
rs2366017
LINC01483
17 69854760 intron variant G/A snv 2.1E-02 2
rs695867
FEN1 ; TMEM258 ; MIR611 ; FADS2
11 61793816 intron variant A/G snv 2.6E-02 1