Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1145652 5 165337081 intergenic variant A/G snv 9.6E-02 1
rs12098564
LINC01519
10 85193571 non coding transcript exon variant A/G snv 7.4E-02 1
rs1225736
LOC101928191 ; SYCP2L
6 10939156 intron variant A/G snv 0.24 1
rs1570069
ELOVL2
6 11017592 intron variant A/G snv 0.54 1
rs16832011
LCT
2 135787729 downstream gene variant A/G snv 5.1E-02 1
rs17648246
LOC107984619
13 44919746 intergenic variant A/G snv 5.0E-02 1
rs197770
ITGA9
3 37474336 intron variant A/G snv 0.12 1
rs2147041
ELOVL2-AS1
6 11050290 intron variant A/G snv 0.53 1
rs2281591
ELOVL2
6 10990260 intron variant A/G snv 0.30 1
rs2295600
SYCP2L
6 10962017 intron variant A/G snv 0.45 1
rs2453710
RPLP0P2
11 61639070 non coding transcript exon variant A/G snv 0.45 1
rs2585617 6 68627895 non coding transcript exon variant A/G snv 0.90 1
rs3798709
ELOVL2
6 11001043 intron variant A/G snv 0.18 1
rs3798722
ELOVL2
6 11040190 intron variant A/G snv 0.39 1
rs6456745
SYCP2L
6 10894035 intron variant A/G snv 0.36 0.38 1
rs695867
FEN1 ; TMEM258 ; MIR611 ; FADS2
11 61793816 intron variant A/G snv 2.6E-02 1
rs7435
AGPAT3
21 43984457 3 prime UTR variant A/G snv 0.35 1
rs7743830
ELOVL2
6 11013987 intron variant A/G snv 0.54 1
rs870288
RBFOX1
16 5535851 intron variant A/G snv 0.30 1
rs9295764
ELOVL2 ; ELOVL2-AS1
6 11044963 non coding transcript exon variant A/G snv 0.59 1
rs9357021
SYCP2L
6 10905921 intron variant A/G snv 0.23 1
rs9393800
SYCP2L ; LOC101928191
6 10951504 intron variant A/G snv 0.20 1
rs9461310
SYCP2L
6 10919963 intron variant A/G snv 0.31 1
rs17156426
FADS2
11 61841851 intron variant A/G;T snv 2
rs1225717
SYCP2L
6 10978007 intron variant A/G;T snv 1