Variant (rsID / SNP)

rs34780140

rs34780140 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBBP8. Location: chromosome 18, position 20,573,434. Clinical significance in the table: Benign.

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Reference-table entries

RBBP8Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:20573434
Cytoband: 18q11.2
HGVS: NM_002894.3(RBBP8):c.1644T>C (p.Asp548=)
Allele change: Synonymous_D548D

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.