Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24 15
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174594
FADS2
0.776 0.160 11 61852357 intron variant C/A;T snv 14
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 12
rs6330
NGF ; NGF-AS1
0.763 0.240 1 115286692 missense variant G/A snv 0.37 0.36 12
rs2230774
ROCK2
0.807 0.240 2 11218994 missense variant G/C;T snv 0.49 12
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs104894833
RPL36A-HNRNPH2 ; GLA
0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 10
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs11739136
KCNIP1 ; KCNMB1
0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10