Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10237735
PDE1C
7 32337136 intron variant C/T snv 7.6E-02 2
rs10414689 19 51293045 regulatory region variant T/C snv 0.11 2
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2
rs1061808
PPT2 ; EGFL8 ; AGPAT1 ; PPT2-EGFL8
6 32168770 3 prime UTR variant T/G snv 0.64 2
rs10809457
LOC105375974
9 11402319 intron variant G/T snv 0.36 2
rs108499
TMEM258 ; MYRF
11 61779765 intron variant C/T snv 0.27 2
rs10885997
PNLIPRP2
10 116638460 synonymous variant A/G snv 0.38 0.36 2
rs1109748
LOC107984334 ; BEST1
11 61955173 synonymous variant C/A snv 0.21 0.11 2
rs11119805
LPGAT1
1 211744902 3 prime UTR variant T/A snv 0.13 2
rs11120822
CAMTA1
1 7053052 intron variant G/C snv 0.34 2
rs11190604
HIF1AN
10 100542700 intron variant A/G snv 0.19 2
rs11230815 11 61868654 downstream gene variant G/C;T snv 2
rs12098564
LINC01519
10 85193571 non coding transcript exon variant A/G snv 7.4E-02 2
rs12529874 6 98014625 intron variant G/A snv 2.6E-02 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
rs146524044
MYO5B
18 50057046 intron variant A/C snv 1.0E-03 2
rs149803
MYRF ; TMEM258
11 61771548 synonymous variant C/G;T snv 0.18 2
rs151159962
SKA1
18 50386938 intron variant T/C snv 1.3E-03 2
rs17156426
FADS2
11 61841851 intron variant A/G;T snv 2
rs17156442
FADS2
11 61846551 intron variant C/T snv 0.11 2
rs174449 11 61872907 downstream gene variant G/A snv 0.54 2
rs174456
FADS3
11 61888710 intron variant C/A snv 0.59 2
rs174464
FADS3
11 61890454 intron variant A/G snv 0.59 2
rs174468 11 61896219 upstream gene variant G/A snv 0.28 2