Variant (rsID / SNP)

rs1236913

rs1236913 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTGS1. Location: chromosome 9, position 125,133,479. The table records no clinical significance for this variant.

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Reference-table entries

PTGS1Not classified

Variant type: missense_variant
Chromosome / position: 9:125133479
HGVS: NM_000962.4,c.22T>C,p.Trp8Arg
Allele change: Silent

Associated conditions / phenotypes

Inflammatory Spondylopathy|Spondyloarthropathy 1|Bone Resorption Disease|Spondylitis

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.