Variant (rsID / SNP)

rs58760581

rs58760581 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC6. Location: chromosome 16, position 16,248,476. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ABCC6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:16248476
Cytoband: 16p13.11
HGVS: NM_001171.6(ABCC6):c.4208+9G>A
Allele change: Silent

Associated conditions / phenotypes

Pseudoxanthoma elasticum|Arterial calcification, generalized, of infancy, 2|Pseudoxanthoma elasticum, forme fruste

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.