Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 3
rs1007323
LOC101928191 ; SYCP2L
6 10953011 intron variant T/A;G snv 1
rs10220265 13 103397233 downstream gene variant G/A snv 0.28 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs10237735
PDE1C
7 32337136 intron variant C/T snv 7.6E-02 2
rs10404486
ZNF600
19 52780882 non coding transcript exon variant C/T snv 0.20 1
rs10414689 19 51293045 regulatory region variant T/C snv 0.11 2
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2
rs1058694
AGPAT3
21 43984239 3 prime UTR variant C/T snv 0.32 1
rs1061808
PPT2 ; EGFL8 ; AGPAT1 ; PPT2-EGFL8
6 32168770 3 prime UTR variant T/G snv 0.64 2
rs10769780
SYT9
11 7345864 intron variant T/C snv 0.25 1
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39 3
rs10792320 11 61978819 intergenic variant A/C;T snv 1
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
rs10897208 11 62024415 intergenic variant A/T snv 0.11 1
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
rs11230874 11 62028114 intergenic variant T/G snv 6.9E-02 1