Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61871342
BLOC1S2
1.000 0.040 10 100278884 intron variant G/A snv 0.36 2
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31 5
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs7637230
LINC02085
0.925 0.040 3 101944711 intron variant A/G;T snv 2
rs4851529
LOC107985926
0.827 0.120 2 102030838 downstream gene variant G/A snv 0.44 5
rs871656
IL1R1
0.827 0.120 2 102154822 intron variant T/A;C snv 5
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 9
rs1020760
NFKB1
0.925 0.040 4 102593288 non coding transcript exon variant C/G snv 0.42 2
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 6
rs12972990
ICAM5
1.000 0.040 19 10295755 intron variant T/G snv 0.35 1
rs73510898
ZGLP1
0.925 0.120 19 10305768 intron variant G/A;C;T snv 2
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 6
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs1002212321
RIMS2
1.000 0.040 8 103931366 missense variant T/C snv 1
rs527418169
LOC105375688 ; RIMS2
1.000 0.040 8 104093501 missense variant G/A;T snv 4.4E-06; 4.4E-06 1
rs11053802
KLRC1
1.000 0.040 12 10444608 intron variant C/G;T snv 1
rs1051738
PDE4A
1.000 0.040 19 10467167 missense variant C/A;T snv 0.17; 4.8E-05 1
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14