Variant (rsID / SNP)

rs111866313

rs111866313 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTGER4. Location: chromosome 5, position 40,691,893. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PTGER4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:40691893
Cytoband: 5p13.1
HGVS: NM_000958.3(PTGER4):c.880G>A (p.Val294Ile)
Allele change: Missense_V294I

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.