Source: INFERRED ×
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 14
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 8
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 8
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 7
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 6
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 6
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 5
rs12042319
DOCK7
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 5
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 5
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs17475879 0.925 0.040 6 30396731 regulatory region variant C/T snv 5.6E-02 5
rs2384550 1.000 0.040 12 114914926 regulatory region variant G/A snv 0.33 5
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv 5
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 5
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 5