Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 7