Variant (rsID / SNP)

rs2235112

rs2235112 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DLGAP2. Location: chromosome 8, position 1,616,718. The table records no clinical significance for this variant.

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Reference-table entries

DLGAP2Not classified

Variant type: synonymous_variant
Chromosome / position: 8:1616718
HGVS: NM_001346810.2,c.2034A>G,p.Glu678Glu
Allele change: Synonymous_E678E

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.