Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs11125080
ATP6V1E2
0.882 0.040 2 46505266 intron variant G/A;C snv 3
rs1150754
TNXB
0.851 0.200 6 32082981 intron variant C/A;T snv 3
rs116427960
HLA-B
0.925 0.120 6 31351449 intron variant C/G;T snv 3
rs12052005
CCDC102B
0.882 0.040 18 68832311 intron variant G/C;T snv 3
rs12128108
AGBL4
0.925 0.040 1 49827749 intron variant C/G;T snv 3
rs138449918
SLC8A1-AS1
0.882 0.040 2 39936810 intron variant AT/-;ATAT delins 3
rs138488080 0.882 0.120 6 29638984 upstream gene variant G/A snv 3
rs169738
GGNBP1
1.000 0.040 6 33569769 intron variant A/G;T snv 3
rs1975802
PLA2G15
1.000 0.040 16 68251944 intron variant A/C;G snv 3
rs221798
GIGYF1
0.882 0.040 7 100689872 intron variant C/A;G snv 3
rs2535627 1.000 0.040 3 52811089 downstream gene variant T/A;C;G snv 3
rs268134
SPRED2
0.925 0.120 2 65381229 intron variant A/C;G;T snv 3
rs28437878
HYKK
1.000 0.040 15 78515530 intron variant C/G;T snv 3
rs3027001
CADM3-AS1 ; CADM3
1.000 0.040 1 159199673 intron variant C/G;T snv 3
rs3747631
LOC105371692 ; LRRN2
1.000 0.040 1 204618441 missense variant G/A;C snv 4.0E-06; 0.20 3
rs4664442
SLC4A10
1.000 0.040 2 161971491 intron variant G/A;C snv 3
rs4702
FES ; FURIN
1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv 3
rs6558872
CSMD1
0.882 0.040 8 4380617 intron variant G/A;C snv 3
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv 3
rs72986630
ZNF823
1.000 0.040 19 11738921 5 prime UTR variant C/A;T snv 3
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs7766730 0.882 0.040 6 65987110 intergenic variant C/A;T snv 3
rs875989808
SYNGAP1
0.925 0.160 6 33444529 missense variant C/T snv 3