Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs7439186

AMBN

rs7439186 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AMBN. Location: chromosome 4, position 71,469,604. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

AMBNNot classified
Variant type
missense_variant
Chromosome / position
4:71469604
HGVS
NM_016519.6,c.764C>T,p.Ala255Val
Allele change
Missense_A255V

Associated conditions / phenotypes

Dental Caries

Public references

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