Disease: Child Development Disorders, Pervasive
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs2799573
CACNB2
0.851 0.040 10 18312999 intron variant T/C snv 0.20 5
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 3
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs3132581
MUCL3 ; HCG21 ; SFTA2
0.851 0.040 6 30945681 intron variant G/A snv 9.3E-02 5
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 6
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 7
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs1715
ZNF615
0.851 0.040 19 51991525 3 prime UTR variant T/C snv 1.4E-05 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 5