Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292661
PDIA5
1.000 0.080 3 123150263 missense variant C/G;T snv 8.2E-04 3
rs2910829
PDE4D
0.925 0.080 5 60174072 intron variant G/A snv 0.52 3
rs3093135
CYP4F2
0.925 0.080 19 15893561 intron variant A/T snv 0.15 3
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 3
rs4044210
CELSR1
0.925 0.080 22 46390418 missense variant T/A;C snv 4.0E-06; 0.17 3
rs42039
CDK6
1.000 0.080 7 92615108 3 prime UTR variant C/T snv 0.19 0.19 3
rs4471613
ALDH1A2
1.000 0.080 15 58259495 intron variant G/A snv 4.3E-02 3
rs4742170
LOC107987046 ; IL33
0.925 0.080 9 6242950 intron variant C/G;T snv 3
rs6007897
CELSR1
0.925 0.080 22 46384624 missense variant T/C snv 0.16 0.28 3
rs6825454 1.000 0.080 4 154580036 downstream gene variant T/C snv 0.25 3
rs764522
TGFBR2 ; LOC105377015
0.882 0.080 3 30605058 upstream gene variant G/A;C snv 3
rs768349387
ADRB2
1.000 0.080 5 148827850 missense variant T/C snv 8.0E-06 3
rs7859727
CDKN2B-AS1
1.000 0.080 9 22102166 intron variant C/T snv 0.57 3
rs796145467
LDLR
0.925 0.080 19 11123310 synonymous variant C/T snv 4.0E-06 2.1E-05 3
rs867671924
ITGB3
1.000 0.080 17 47292176 missense variant C/A snv 3
rs876537
CRPP1
1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 3
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 3
rs978906
ROCK2
0.925 0.080 2 11183150 3 prime UTR variant T/A;C snv 3
rs10435816
IL33
1.000 0.080 9 6225535 intron variant A/G snv 0.35 2
rs10947803
KCNK17
1.000 0.080 6 39302834 intron variant C/A snv 2
rs11018628
NOX4
1.000 0.080 11 89473343 intron variant T/C;G snv 2
rs11196288 1.000 0.080 10 113297684 regulatory region variant A/G snv 5.5E-02 2
rs11237379
NDUFC2-KCTD14 ; NDUFC2
1.000 0.080 11 78074911 intron variant T/C snv 0.38 2
rs11265260 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 2
rs11957829
LOC100505841
1.000 0.080 5 122179500 intron variant A/G snv 0.18 0.19 2