Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 7
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs7195830
CYBA
0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69 6
rs73885319
APOL1
0.851 0.120 22 36265860 missense variant A/G snv 1.6E-02 6.6E-02 6
rs13538
NAT8 ; ALMS1P1
1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 5
rs371237692
REN
0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05 5
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29 5
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs174530
MYRF ; TMEM258
1.000 0.080 11 61779120 non coding transcript exon variant A/G snv 0.30 4
rs174564
FADS2 ; FADS1
1.000 0.080 11 61820833 intron variant A/G snv 0.30 4
rs174592
FADS2
1.000 0.080 11 61851136 intron variant A/G snv 0.44 4
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 3
rs174562
FADS2 ; FADS1
1.000 0.080 11 61817672 intron variant A/G snv 0.28 3
rs11662622 1.000 0.080 18 65592400 intergenic variant A/G snv 0.20 2
rs1551122
OTOGL
1.000 0.080 12 80372020 missense variant A/G snv 0.58 0.50 2
rs2074381
ALPK1
4 112432293 missense variant A/G snv 8.5E-03 5.5E-03 2
rs2404298
DLGAP2
1.000 0.080 8 1420853 intron variant A/G snv 0.84 2
rs447707
KIRREL2 ; NPHS1
1.000 0.080 19 35856498 intron variant A/G snv 0.20 2
rs4725366
AOC1 ; LOC105375567
1.000 0.080 7 150824966 splice region variant A/G snv 0.81 2
rs9846911 3 187500548 intergenic variant A/G snv 0.47 2
rs2271683
COL3A1
2 189009011 missense variant A/G snv 4.4E-03 1.6E-03 1