Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs130078

CCHCR1

rs130078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCHCR1. Location: chromosome 6, position 31,118,565. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

CCHCR1Not classified
Variant type
synonymous_variant
Chromosome / position
6:31118565
HGVS
NM_001394641.1,c.1065G>C,p.Val355Val
Allele change
Synonymous_V310V

Public references

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