Variant (rsID / SNP)

rs63750459

rs63750459 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC6. Location: chromosome 16, position 16,256,967. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

ABCC6Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 16:16256967
Cytoband: 16p13.11
HGVS: NM_001171.6(ABCC6):c.3389C>T (p.Thr1130Met)
Allele change: Silent

Associated conditions / phenotypes

Pseudoxanthoma elasticum|Abnormality of the eye

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.