Disease: Fatty acid measurement
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
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
rs334809
IL5RA
0.925 0.080 3 3088537 intron variant A/G;T snv 4
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
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
rs17648246
LOC107984619
13 44919746 intergenic variant A/G snv 5.0E-02 2
rs2118674
MYO3B
2 170462384 intron variant A/T snv 0.87 2
rs2366017
LINC01483
17 69854760 intron variant G/A snv 2.1E-02 2
rs2391388
ALG14
1 95020269 intron variant A/C snv 0.49 2
rs3134950
PPT2 ; PPT2-EGFL8
6 32159700 intron variant C/A snv 0.64 2
rs4465599
SHISA9
16 13061021 intron variant G/A snv 0.69 2
rs6671200
TLCD4-RWDD3 ; LOC101928118
1 95231973 intron variant A/C snv 0.90 2
rs6675668
ALG14
1 95050081 intron variant T/G snv 0.43 2