Variant (rsID / SNP)

rs41281120

rs41281120 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCCA. Location: chromosome 13, position 100,955,204. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PCCAConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 13:100955204
Cytoband: 13q32.3
HGVS: NM_000282.4(PCCA):c.1236A>G (p.Pro412=)
Allele change: Synonymous_P97P

Associated conditions / phenotypes

Propionic acidemia

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.