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Variant (rsID / SNP)

rs610037

AP5B1

rs610037 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AP5B1. Location: chromosome 11, position 65,546,857. The table records no clinical significance for this variant.

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Reference-table entries

AP5B1Not classified
Variant type
synonymous_variant
Chromosome / position
11:65546857
HGVS
NM_138368.5,c.1107T>G,p.Leu369Leu
Allele change
Synonymous_L369L

Public references

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