Variant (rsID / SNP)

rs3825569

rs3825569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RTL1. Location: chromosome 14, position 101,350,298. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

RTL1Not classified

Variant type: synonymous_variant
Chromosome / position: 14:101350298
HGVS: NM_001134888.3,c.828A>G,p.Glu276Glu
Allele change: Synonymous_E276E

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.