Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs330261

PRR5L

rs330261 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRR5L. Location: chromosome 11, position 36,422,792. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

PRR5LNot classified
Variant type
missense_variant
Chromosome / position
11:36422792
HGVS
NM_001160167.2,c.121G>A,p.Ala41Thr
Allele change
Missense_A41T

Public references

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