Variant (rsID / SNP)

rs7280643

rs7280643 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBM11. Location: chromosome 21, position 15,599,466. The table records no clinical significance for this variant.

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Reference-table entries

RBM11Not classified

Variant type: missense_variant
Chromosome / position: 21:15599466
HGVS: NM_001320602.2,c.719A>G,p.His240Arg
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.