Variant (rsID / SNP)

rs16889042

rs16889042 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD21. Location: chromosome 8, position 117,879,001. Clinical significance in the table: Likely benign.

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Reference-table entries

RAD21Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 8:117879001
Cytoband: 8q24.11
HGVS: NM_006265.3(RAD21):c.-32-1G>A
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.