Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3176867
VCAM1
1 100728649 intron variant C/A;T snv 1
rs1044486
USP36
17 78796097 3 prime UTR variant G/A snv 0.41 1
rs1186699
USP34
2 61435420 intron variant C/A snv 0.32 1
rs2774279
USF1 ; ARHGAP30
0.925 0.080 1 161047766 synonymous variant C/T snv 0.27 0.27 3
rs3752105
UPF3A ; LOC105370384
13 114281830 missense variant G/A;C snv 0.23; 2.7E-05 1
rs7694531
UNC5C
4 95165950 3 prime UTR variant A/G snv 0.64 2
rs2290769
UNC13D
17 75830325 intron variant G/A;C snv 4.9E-06; 0.18 1
rs12972366
UHRF1
19 4920402 intron variant A/G snv 0.29 1
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs10500326
UBN1
16 4868325 intron variant G/T snv 0.21 1
rs7129204
UBASH3B
11 122656504 intron variant G/C snv 0.15 1
rs34042070
TXNL4B ; HPR
16 72067626 intron variant C/G snv 0.17 4
rs463312
TUBB1
1.000 0.040 20 59022915 missense variant A/C snv 7.7E-02 5.7E-02 4
rs1234442507
TUBB1
1.000 0.040 20 59022915 frameshift variant AG/- del 4.0E-06 3
rs11111839
TTC41P
12 103916945 intron variant C/A snv 7.9E-02 1
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 14
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 8
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs17819305
TNC ; DELEC1
9 115053951 intron variant C/T snv 5.6E-02 1
rs7099692
TMEM72-AS1
10 44896515 intron variant G/A;C snv 1
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4704825
TIMD4
5 156955297 intron variant A/G snv 0.56 1