Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs12711521
MASP2 ; TARDBP
0.807 0.240 1 11030859 missense variant C/A snv 0.74 0.63 7
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 7
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs1514175
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1.000 0.080 1 74525960 intron variant A/G snv 0.48 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs34720381
PRRC2C
1 171486183 intron variant C/T snv 7.3E-02 4
rs545608
CRYZL2P-SEC16B ; SEC16B
0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 3
rs10923724 1 119004219 upstream gene variant C/T snv 0.53 3
rs11209951
LOC105378797
1 72371807 intron variant C/T snv 0.61 3
rs113722913
LOC105371682
1 199950846 intergenic variant T/C snv 2.6E-02 3