Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519831
PLCG2
1.000 0.120 16 81912655 missense variant C/T snv 3
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 3
rs2292982
IRF8
1.000 0.120 16 85911217 intron variant T/C;G snv 3
rs539846
BMF
1.000 0.120 15 40105735 intron variant G/C;T snv 2
rs1041569
TNFSF13B
1.000 0.120 13 108267195 intron variant T/A;C snv 1
rs1057519832
PLCG2
1.000 0.120 16 81928578 missense variant A/C;G;T snv 1
rs1064796681
TP53
1.000 0.120 17 7675091 missense variant C/T snv 1
rs11688943
PPIL3
1.000 0.120 2 200875545 intron variant T/C snv 0.30 1
rs1278359106
IRAK4
1.000 0.120 12 43777710 missense variant C/T snv 4.0E-06 7.0E-06 1
rs1349826807
TERF2IP ; KARS1
1.000 0.120 16 75648280 missense variant G/A snv 7.9E-05 4.2E-05 1
rs143635917
POT1
1.000 0.120 7 124842843 missense variant T/C snv 4.5E-04 4.1E-04 1
rs146850453
ARL11
1.000 0.120 13 49630937 missense variant G/A;C snv 3.7E-04; 4.1E-06 1
rs17676986
SND1 ; SND1-IT1 ; LOC105375492
1.000 0.120 7 127996905 intron variant C/T snv 0.12 1
rs1776948
SLC23A2
1.000 0.120 20 4950467 intron variant G/A;C snv 1
rs2147420
FAS
1.000 0.120 10 88999856 intron variant A/G snv 0.50 1
rs2266690
CCNH
1.000 0.120 5 87399457 missense variant A/G;T snv 1
rs228014
ASTN1
1.000 0.120 1 177002472 intron variant T/C snv 0.58 1
rs2307842
C12orf73 ; HSP90B1
1.000 0.120 12 103947867 3 prime UTR variant GACT/-;GACTGACT delins 0.15 1
rs2466032
CASC19 ; PCAT1
1.000 0.120 8 127197575 non coding transcript exon variant T/C snv 0.23 1
rs2705511
LOC112268446
1.000 0.120 3 112460632 downstream gene variant A/C;G snv 1
rs3136687
CCR7
1.000 0.120 17 40561644 intron variant T/C snv 0.18 1
rs35748167 1.000 0.120 18 60370200 intron variant G/C;T snv 1
rs369203092
ATM
1.000 0.120 11 108247117 missense variant T/C snv 8.0E-06 1
rs371713984
ATM
1.000 0.120 11 108247110 missense variant G/A;C snv 8.0E-06; 4.0E-06 1
rs3805500
DROSHA
1.000 0.120 5 31462870 intron variant G/A snv 0.60 1