Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs140226130
CCDC178
0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs3825214
TBX5
0.851 0.080 12 114357638 intron variant G/A snv 0.77 8
rs16867253
GRHL1
0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7
rs7961581
TSPAN8
0.827 0.200 12 71269322 intron variant C/T snv 0.75 7
rs10163755
DSG4 ; DSG1-AS1
0.827 0.200 18 31405413 intron variant G/A snv 0.74 6
rs11708996
SCN5A
0.925 0.120 3 38592432 intron variant G/C snv 0.11 6
rs4385527
AOPEP
0.827 0.280 9 94886305 intron variant G/A snv 0.31 6
rs12908437
IGF1R
0.882 0.200 15 98744146 intron variant T/C;G snv 5
rs1492099
AGTR1
0.882 0.120 3 148719716 intron variant T/A;C snv 0.89 5
rs1860561
ATP2A2
0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs498005
HCN4
0.851 0.160 15 73327969 intron variant C/T snv 0.48 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
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 4
rs2244613
CES1
0.882 0.120 16 55810697 intron variant G/A;T snv 8.0E-06; 0.73 4
rs4240157
ACE2
0.925 0.080 X 15568841 intron variant C/T snv 4
rs4647602
CASP3 ; PRIMPOL
0.925 0.120 4 184648647 intron variant G/T snv 9.5E-02 4
rs6632677
ACE2
0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 4