Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7626962
SCN5A
0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs3825214
TBX5
0.851 0.080 12 114357638 intron variant G/A snv 0.77 8
rs1860561
ATP2A2
0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs398122917
CLIC2
0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 5
rs740363
HSPA12A
0.851 0.080 10 116816095 intron variant G/A snv 0.40 5
rs10465885
LOC102723321 ; GJA5
0.882 0.080 1 147760632 intron variant T/A;C snv 4
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 4
rs16971436
ZFHX3
0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02 4
rs17287293
LOC105369698
1.000 0.080 12 24617944 intergenic variant A/G snv 0.12 4
rs199472708
KCNQ1
0.882 0.080 11 2572015 missense variant G/A snv 4
rs2549513
MAF
0.851 0.080 16 79516830 downstream gene variant C/A;T snv 4
rs4240157
ACE2
0.925 0.080 X 15568841 intron variant C/T snv 4
rs499818 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 4
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14 3
rs121918603
RYR2
0.882 0.080 1 237639068 missense variant C/T snv 3
rs1253810269
ARID1A
0.882 0.080 1 26696971 missense variant G/A snv 7.0E-06 3
rs1273246817
RYR2
0.882 0.080 1 237784169 missense variant A/C snv 3
rs12932445
ZFHX3
0.925 0.080 16 73035989 intron variant T/C snv 0.18 3
rs147750704
KCNJ2
0.925 0.080 17 70175316 missense variant G/A snv 1.6E-04 7.0E-05 3
rs1805120
KCNH2
0.882 0.080 7 150952443 synonymous variant G/A snv 0.30 0.26 3
rs220733
MAS1
1.000 0.080 6 159897771 intron variant A/C;G snv 0.99 3
rs332388
SLC25A26
1.000 0.080 3 66361431 intron variant T/C snv 0.55 3
rs4642101
CAND2
1.000 0.080 3 12800724 intron variant T/G snv 0.63 3
rs4646155
ACE2
0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02 3