Variant (rsID / SNP)

rs55893495

rs55893495 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERVFRD-1, SMIM13. Location: chromosome 6, position 11,104,251. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ERVFRD-1Not classified

Variant type: synonymous_variant
Chromosome / position: 6:11104251
HGVS: NM_207582.3,c.1293T>C,p.Cys431Cys
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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