Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11787216
rs11787216
1.000 0.040 8 141605122 intron variant C/T snv 0.26
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.700 1.000 1 2019 2019
dbSNP: rs13294439
rs13294439
1.000 0.040 9 23358877 intron variant A/C snv 0.32
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.700 1.000 1 2019 2019
dbSNP: rs1452075
rs1452075
1.000 0.040 3 62495388 intron variant C/T snv 0.73
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.700 1.000 1 2019 2019
dbSNP: rs2388334
rs2388334
0.882 0.040 6 98143746 intron variant A/G snv 0.39
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.700 1.000 1 2019 2019
dbSNP: rs2898883
rs2898883
PHB
1.000 0.040 17 49405591 intron variant G/A snv 0.23
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.700 1.000 1 2018 2018