Variant (rsID / SNP)

rs115158839

rs115158839 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPOX. Location: chromosome 1, position 161,136,320. Clinical significance in the table: Likely benign.

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Reference-table entries

PPOXLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:161136320
Cytoband: 1q23.3
HGVS: NM_001122764.3(PPOX):c.-151G>T
Allele change: Silent

Associated conditions / phenotypes

Variegate porphyria

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.