Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3858145 0.882 0.040 10 68252081 regulatory region variant A/G snv 0.33 3
rs200208925
MYOC
0.925 0.040 1 171652454 missense variant A/G snv 6.4E-05 2.1E-05 2
rs2022945 1.000 0.040 8 107238911 intergenic variant A/G snv 0.87 2
rs3213787
SRBD1
0.925 0.040 2 45419685 intron variant A/G snv 4.3E-02 2
rs34595252
WDR36
0.925 0.040 5 111119021 missense variant A/G snv 4.3E-03 4.5E-03 2
rs58073046
ARHGEF12
1.000 0.040 11 120377784 intron variant A/G snv 8.7E-02 2
rs12699251
THSD7A
1.000 0.040 7 11639486 intron variant A/G snv 0.33 1
rs56233426 1.000 0.040 3 186411027 intergenic variant A/G snv 0.50 1
rs61861119 1.000 0.040 10 93182666 intergenic variant A/G snv 0.45 1
rs774766411
CXCL8
1.000 0.040 4 73741625 missense variant A/G snv 1.2E-05 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2935057 1.000 0.040 6 170139691 intron variant A/G;T snv 1
rs542340
DNAJC24
1.000 0.040 11 31387891 intron variant A/G;T snv 5.5E-03 1
rs8141433 1.000 0.040 22 19866483 intergenic variant A/G;T snv 1
rs197388
INKA2 ; DDX20 ; LOC101928718
0.925 0.040 1 111754860 non coding transcript exon variant A/T snv 0.27 2
rs4243042
LOXL1
1.000 0.040 15 73949283 intron variant A/T snv 0.37 1
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs74315339
MYOC
0.807 0.120 1 171652468 missense variant C/A snv 9.8E-04 1.3E-04 6
rs11656696
GAS7
0.882 0.040 17 10130362 intron variant C/A snv 0.36 5
rs121918071
TTR
0.882 0.240 18 31595209 missense variant C/A snv 4
rs7555523
TMCO1
0.925 0.040 1 165749742 intron variant C/A snv 0.88 4
rs786204848
DDX58
0.882 0.040 9 32488884 missense variant C/A snv 4
rs643319
CDKN2B-AS1
0.882 0.080 9 22017837 intron variant C/A snv 0.40 3
rs12154178
ESR1
0.925 0.040 6 151929945 intron variant C/A snv 0.59 2