Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs4453265

C2CD3

rs4453265 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2CD3. Location: chromosome 11, position 73,785,326. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

C2CD3Not classified
Variant type
synonymous_variant
Chromosome / position
11:73785326
HGVS
NM_001286577.2,c.4923A>G,p.Val1641Val
Allele change
Synonymous_V1641V

Public references

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