Variant (rsID / SNP)

rs141586518

rs141586518 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ESRRB. Location: chromosome 14, position 76,906,047. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ESRRBConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 14:76906047
Cytoband: 14q24.3
HGVS: NM_001379180.1(ESRRB):c.414G>A (p.Val138=)
Allele change: Synonymous_V117V

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.