Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4100654
ABCA1
9 104906960 intron variant T/C snv 8.3E-02 3
rs2777795
ABCA1
9 104910084 intron variant G/A snv 8.8E-02 3
rs10271556
NAMPT
7 106258428 intron variant C/T snv 5.6E-02 4
rs12247406
SORCS1
10 106996746 intron variant G/A snv 1.3E-02 3
rs480392
NTNG1
1 107436774 synonymous variant A/C snv 0.99 0.95 3
rs4987897
ATM
11 108227415 5 prime UTR variant C/T snv 1.4E-02 2
rs3218688
ATM
11 108268595 missense variant C/T snv 3.2E-05 2.1E-05 4
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
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
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs2075440
MYO1H
12 109421295 intron variant A/G snv 0.51 2
rs2338104
KCTD10
1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58 3
rs7134594
MMAB
1.000 0.200 12 109562388 intron variant C/G;T snv 2
rs7998875
COL4A1
13 110289053 intron variant G/A;T snv 3
rs11065633
ATP2A2
12 110348445 3 prime UTR variant C/T snv 2.3E-02 2
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs2238894
ARHGAP6
X 11146710 intron variant G/A snv 1.6E-03 2
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs12979813
DOCK6
19 11232027 intron variant A/G snv 0.30 2
rs737337
DOCK6
0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 2