Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs2470893
CYP1A1
0.882 0.160 15 74727108 upstream gene variant C/T snv 0.20 8
rs1613662
GP6 ; LOC107985325
0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 8
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 6
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 5
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs8176685
ABO
9 133263363 intron variant CACCACTACGCC/- delins 4
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs4432538
PLCB1 ; LOC105372521
20 8626746 intron variant G/A snv 0.52 4
rs374039502
TNFSF13B
0.925 0.160 13 108308037 3 prime UTR variant T/A snv 2.0E-02 4
rs117672662
ACTN1
14 68958750 intron variant T/C snv 7.4E-03 3
rs17572109
ARPC2
2 218229211 non coding transcript exon variant G/A;T snv 3
rs2901656
C1orf105
1 172465672 3 prime UTR variant C/A;T snv 0.51 3
rs553749201
CHRNE ; GP1BA
17 4933900 synonymous variant C/A snv 3
rs139141690
CUX1
7 101856650 intron variant G/A snv 2.2E-03 3
rs655029
EHD3
2 31254972 intron variant G/A snv 0.78 3
rs41315846
GCSAML
1 247549001 intron variant T/C snv 0.44 0.52 3
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3