Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 12
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 7
rs13431652
SPC25
0.925 0.080 2 168896905 intron variant T/C snv 0.24 5
rs174545
FADS1 ; FADS2
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28 5
rs2880301
TPTE2
1.000 0.040 13 19526394 intron variant C/T snv 4
rs334809
IL5RA
0.925 0.080 3 3088537 intron variant A/G;T snv 4
rs987052
LINC02135 ; LINC01081
16 86288853 intron variant T/C snv 0.23 3
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
rs10809457
LOC105375974
9 11402319 intron variant G/T snv 0.36 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
rs113847670
DOCK1
10 127076415 intron variant C/T snv 3.3E-02 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