Variant (rsID / SNP)

rs149189755

rs149189755 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBBP8. Location: chromosome 18, position 20,516,929. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RBBP8Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:20516929
Cytoband: 18q11.2
HGVS: NM_002894.3(RBBP8):c.109+6A>G
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.