Variant (rsID / SNP)

rs41269040

rs41269040 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RPS10. Location: chromosome 6, position 34,386,219. Clinical significance in the table: Benign.

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Reference-table entries

RPS10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:34386219
Cytoband: 6p21.31
HGVS: NM_001014.5(RPS10):c.401-18C>T
Allele change: Silent

Associated conditions / phenotypes

Diamond-Blackfan anemia

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.