Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 5
rs4783961
CETP
0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 3
rs2279238
NR1H3
0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26 2
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 3
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 2
rs1877031
STARD3
0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52 1
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
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
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4