Disease: Child Development Disorders, Pervasive
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10211550
MOB4 ; HSPE1-MOB4
1.000 0.040 2 197518575 intron variant G/T snv 0.37 2
rs1024582
CACNA1C
1.000 0.040 12 2293080 intron variant A/G;T snv 2
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10520163
CLCN3
1.000 0.040 4 169705401 intron variant T/A;C snv 2
rs10791097
LINC02551
1.000 0.040 11 130848735 intron variant T/G snv 0.60 2
rs10791111 1.000 0.040 11 130986204 intergenic variant T/G snv 0.45 2
rs1080500 1.000 0.040 3 53141001 intergenic variant G/A snv 0.27 2
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 5
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs111312615
HLA-A
1.000 0.040 6 29955302 upstream gene variant T/G snv 2
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs111639056
HLA-DRB2
1.000 0.040 6 32570699 intergenic variant G/A snv 0.12 2
rs11191419
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102852578 intron variant T/A snv 0.36 2
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs11191582
NT5C2
1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02 2
rs111977918
HLA-C
1.000 0.040 6 31268274 downstream gene variant G/A;C snv 2
rs11210195
LOC105378800
1.000 0.040 1 73283600 intergenic variant C/T snv 0.44 2
rs11210892 1.000 0.040 1 43634413 intergenic variant G/A snv 0.51 3
rs112209031
HLA-DRB5 ; HLA-DRB3
1.000 0.040 6 32524630 intron variant T/C;G snv 2
rs11223651 1.000 0.040 11 133971139 intergenic variant C/T snv 0.16 2
rs1131275
MIR6891 ; HLA-B
1.000 0.040 6 31356183 missense variant G/A;C snv 0.68 2
rs113205291
HLA-A
1.000 0.040 6 29894844 upstream gene variant A/G;T snv 2
rs113397282
HLA-DRB3 ; HLA-DRB5
1.000 0.040 6 32520273 intron variant T/C;G snv 2
rs114041423 1.000 0.040 6 29639270 upstream gene variant G/A snv 2
rs114086406
TSBP1-AS1
1.000 0.040 6 32374760 intron variant G/A snv 2