Disease: Child Development Disorders, Pervasive
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
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
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 5
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5