Disease: Child Development Disorders, Pervasive
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 3
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 5
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 6
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6