Variant (rsID / SNP)

rs2511841

rs2511841 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF26. Location: chromosome 11, position 119,206,375. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

RNF26Not classified

Variant type: synonymous_variant
Chromosome / position: 11:119206375
HGVS: NM_032015.5,c.543G>A,p.Thr181Thr
Allele change: Synonymous_T181T

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.