Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs10455

CYBRD1

rs10455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYBRD1. Location: chromosome 2, position 172,411,273. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

CYBRD1Not classified
Variant type
missense_variant
Chromosome / position
2:172411273
HGVS
NM_024843.4,c.797G>A,p.Ser266Asn
Allele change
Missense_S208N

Public references

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