Variant (rsID / SNP)

rs55899211

rs55899211 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERVFRD-1, SMIM13. Location: chromosome 6, position 11,105,361. 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: 6:11105361
HGVS: NM_207582.3,c.183G>A,p.Ser61Ser
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.