Variant (rsID / SNP)

rs1143652

rs1143652 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RPL8. Location: chromosome 8, position 146,017,171. The table records no clinical significance for this variant.

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Reference-table entries

RPL8Not classified

Variant type: synonymous_variant
Chromosome / position: 8:146017171
HGVS: NM_000973.5,c.267T>C,p.Tyr89Tyr
Allele change: Synonymous_Y89Y

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.