Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs627928

RNASEL

rs627928 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNASEL. Location: chromosome 1, position 182,551,337. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

RNASELNot classified
Variant type
missense_variant
Chromosome / position
1:182551337
HGVS
NM_021133.4,c.1623T>G,p.Asp541Glu
Allele change
Missense_D541E

Associated conditions / phenotypes

Prostate Cancer

Public references

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