Variant (rsID / SNP)

rs13331553

rs13331553 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RPL3L, MSRB1. Location: chromosome 16, position 1,990,994. The table records no clinical significance for this variant.

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Reference-table entries

RPL3LNot classified

Variant type: downstream_gene_variant
Chromosome / position: 16:1990994
HGVS: NM_005061.3,c.*3844A>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.