Disease: Child Development Disorders, Pervasive
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs190065944
CHRNA5
0.925 0.080 15 78567268 intron variant G/A snv 3.4E-03 5
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs2799573
CACNB2
0.851 0.040 10 18312999 intron variant T/C snv 0.20 5
rs3132581
MUCL3 ; HCG21 ; SFTA2
0.851 0.040 6 30945681 intron variant G/A snv 9.3E-02 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 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
rs707939
MSH5-SAPCD1 ; MSH5
0.851 0.200 6 31758911 intron variant C/A snv 0.34 0.26 5
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs11682175
ACTG1P22
0.925 0.040 2 57760458 intron variant T/C snv 0.38 4
rs13212562 0.925 0.120 6 27332531 intergenic variant A/G snv 0.13 4
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 4
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs11210892 1.000 0.040 1 43634413 intergenic variant G/A snv 0.51 3
rs116427960
HLA-B
0.925 0.120 6 31351449 intron variant C/G;T snv 3
rs11740474
GALNT10
1.000 0.040 5 154301187 intron variant A/T snv 0.37 3
rs12443170
CHRNA3
1.000 0.040 15 78615394 intron variant G/A snv 0.12 3