Disease: Child Development Disorders, Pervasive
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs7907645 1.000 0.040 10 102664043 downstream gene variant T/G snv 0.13 2
rs11191419
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102852578 intron variant T/A snv 0.36 2
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 12
rs11191582
NT5C2
1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02 2
rs12887734
COA8 ; KLC1
1.000 0.040 14 103580497 intron variant G/T snv 0.26 2
rs9879311
ATP2B2
1.000 0.040 3 10373659 intron variant C/A;T snv 2
rs17292804
PPP1R13B
1.000 0.040 14 103738786 synonymous variant G/A snv 8.0E-02 8.5E-02 2
rs8009147
PPP1R13B
1.000 0.040 14 103798325 intron variant A/G;T snv 2
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs41563
SRPK2
1.000 0.040 7 105212207 intron variant G/A;C snv 2
rs4580973
SRPK2
1.000 0.040 7 105263212 intron variant A/G snv 0.45 2
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs427691 1.000 0.040 5 109678809 intergenic variant G/A snv 0.23 2
rs9656169
LOC105375451 ; LOC105375450
1.000 0.040 7 110434219 intron variant C/T snv 0.34 2
rs4642619 1.000 0.040 8 110475239 intergenic variant T/A;G snv 2
rs13240464
IMMP2L
1.000 0.040 7 111258859 intron variant T/C snv 0.34 2
rs4309187 1.000 0.040 11 113541721 intergenic variant A/C snv 0.76 2
rs72986630
ZNF823
1.000 0.040 19 11738921 5 prime UTR variant C/A;T snv 3
rs2851447
MPHOSPH9
1.000 0.040 12 123180566 intron variant G/C snv 0.59 2
rs77502336
GRAMD1B
1.000 0.040 11 123523928 intron variant G/C;T snv 2
rs55661361
NRGN
1.000 0.040 11 124744061 intron variant G/A snv 0.43 3