Variant (rsID / SNP)

rs2710

rs2710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RLBP1. Location: chromosome 15, position 89,753,220. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

RLBP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:89753220
Cytoband: 15q26.1
HGVS: NM_000326.5(RLBP1):c.*296G>A
Allele change: Silent

Associated conditions / phenotypes

Pigmentary retinal dystrophy|Newfoundland cone-rod dystrophy|Retinitis pigmentosa

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.