Variant (rsID / SNP)

rs10879065

rs10879065 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYRFL. Location: chromosome 12, position 70,351,684. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MYRFLNot classified

Variant type: missense_variant
Chromosome / position: 12:70351684
HGVS: NM_182530.3,c.2533C>A,p.Leu845Met
Allele change: Missense_L845M

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.