Variant (rsID / SNP)

rs3752797

rs3752797 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AP1M1. Location: chromosome 19, position 16,339,715. The table records no clinical significance for this variant.

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Reference-table entries

AP1M1Not classified

Variant type: synonymous_variant
Chromosome / position: 19:16339715
HGVS: NM_001130524.2,c.1059C>T,p.Ile353Ile
Allele change: Synonymous_I353I

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.