Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 7
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 5
rs17475879 0.925 0.040 6 30396731 regulatory region variant C/T snv 5.6E-02 5
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 5
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 5
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 4
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 4
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 4
rs4149268
ABCA1
1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
rs10498725
CARMIL1
1.000 0.040 6 25454787 intron variant C/T snv 0.17 3
rs10738609
CDKN2B-AS1
1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 3
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 3
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 3
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 3
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 3
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 3
rs2254287
COL11A2
1.000 0.040 6 33176171 intron variant C/A;G;T snv 3
rs2271293
NUTF2
1.000 0.040 16 67868167 intron variant G/A snv 0.11 3
rs2338104
KCTD10
1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58 3
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 3
rs255049
DPEP3
1.000 0.040 16 67979568 intron variant T/C snv 0.34 3