Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 1
rs3847302
ABCA1
9 104886314 intron variant A/G snv 0.12 2
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 5
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs2777795
ABCA1
9 104910084 intron variant G/A snv 8.8E-02 1
rs2472509
ABCA1
9 104921949 intron variant T/G snv 0.29 1
rs28402213
ARHGEF38
4 105596292 intron variant G/A snv 0.15 1
rs4455790
RP1L1
8 10634174 intron variant C/G snv 0.74 2
rs114529226 14 106368436 upstream gene variant G/A snv 4.3E-02 1
rs2878349 1 107006623 intergenic variant G/A snv 0.28 1
rs752273 2 108314649 upstream gene variant T/A snv 0.23 2
rs750134
CORO1C
12 108667330 intron variant G/T snv 6.8E-02 1
rs884366
CCDC162P
6 109252892 intron variant G/A snv 0.25 1
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 3
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 3
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 1
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs3902354 1 109276674 downstream gene variant C/A;T snv 3