Variant (rsID / SNP)

rs3746120

rs3746120 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APBA3. Location: chromosome 19, position 3,753,769. The table records no clinical significance for this variant.

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Reference-table entries

APBA3Not classified

Variant type: synonymous_variant
Chromosome / position: 19:3753769
HGVS: NM_004886.4,c.1005G>A,p.Ala335Ala
Allele change: Silent

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.