Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs1053667
TOGARAM1
0.925 0.120 14 45073835 3 prime UTR variant T/C snv 0.11 4
rs11337
GOLGA7
0.925 0.120 8 41510767 3 prime UTR variant T/G snv 0.93 4
rs1353759920
TP73
0.851 0.120 1 3707593 missense variant C/A snv 2.1E-05 4
rs4150506
ERCC3
0.851 0.120 2 127262970 intron variant G/A snv 0.18 4
rs3900115
CASP10
1.000 0.120 2 201185954 synonymous variant A/G snv 0.45 0.49 3
rs4901706
TMEM260
1.000 0.120 14 56647667 3 prime UTR variant G/A;C;T snv 3
rs6948
CASP3
1.000 0.120 4 184627976 3 prime UTR variant G/T snv 0.48 3
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs10008492 1.000 0.120 4 38764099 intergenic variant C/G;T snv 2
rs121908689
RAD54L ; LRRC41
0.925 0.120 1 46272758 missense variant T/A snv 2
rs12211228
IRF4
1.000 0.120 6 408833 3 prime UTR variant G/C snv 0.11 2
rs207186 0.925 0.120 1 55359252 intron variant C/T snv 7.7E-03 2
rs2855429
COL11A2
0.925 0.120 6 33190412 intron variant A/C snv 0.78 2
rs3789068
MIR4435-2HG ; BCL2L11
0.925 0.120 2 111151670 intron variant A/G snv 0.41 2
rs3813729
C1RL ; C1R
0.925 0.120 12 7089608 missense variant C/G;T snv 2
rs61733010
AKR1A1
0.925 0.120 1 45561805 missense variant C/G;T snv 4.0E-06; 4.3E-04 1.9E-03 2
rs758837678
NBN ; DECR1
0.925 0.120 8 90001503 missense variant C/T snv 2
rs1003421753
IL12A ; IL12A-AS1
1.000 0.120 3 159989088 missense variant C/T snv 1
rs1039312028
BAX
1.000 0.120 19 48955724 missense variant G/A snv 1.4E-05 1
rs114216685
RAD54B ; FSBP
1.000 0.120 8 94391640 missense variant T/C snv 8.8E-04 3.9E-04 1
rs1163350491
OCM
1.000 0.120 7 5880922 synonymous variant C/T snv 4.0E-06 1
rs1185926926
SLC19A1
1.000 0.120 21 45531748 missense variant A/G snv 4.1E-06 1
rs1250480918
SLC19A1
1.000 0.120 21 45537803 synonymous variant G/A snv 4.6E-06 1