Variant (rsID / SNP)

rs75123867

rs75123867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC50. Location: chromosome 3, position 191,093,285. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CCDC50Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:191093285
Cytoband: 3q28
HGVS: NM_178335.3(CCDC50):c.883G>T (p.Asp295Tyr)
Allele change: Silent

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.