Variant (rsID / SNP)

rs2942133

rs2942133 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPP1R15B. Location: chromosome 1, position 204,369,875. The table records no clinical significance for this variant.

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Reference-table entries

PPP1R15BNot classified

Variant type: downstream_gene_variant
Chromosome / position: 1:204369875
HGVS: NM_032833.5,c.*5345A>C

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.