Variant (rsID / SNP)

rs2301963

rs2301963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DLGAP2. Location: chromosome 8, position 1,514,009. The table records no clinical significance for this variant.

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Reference-table entries

DLGAP2Not classified

Variant type: missense_variant
Chromosome / position: 8:1514009
HGVS: NM_001346810.2,c.1391C>A,p.Pro464Gln
Allele change: Missense_P464Q

Associated conditions / phenotypes

Autism|Autism Spectrum Disorder

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.