Disease: Phospholipid measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 3
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 3