Variant (rsID / SNP)

rs11125529

rs11125529 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACYP2. Location: chromosome 2, position 54,475,866. Clinical significance in the table: association.

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Reference-table entries

ACYP2Association

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 2:54475866
Cytoband: 2p16.2
HGVS: NM_001320586.2(ACYP2):c.405-55959C>A
Allele change: Silent

Associated conditions / phenotypes

Chronic osteomyelitis

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.