Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs3800326

PGBD1

rs3800326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PGBD1. Location: chromosome 6, position 28,264,717. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

PGBD1Not classified
Variant type
missense_variant
Chromosome / position
6:28264717
HGVS
NM_001184743.2,c.767C>T,p.Pro256Leu
Allele change
Missense_P256L

Public references

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