Variant (rsID / SNP)

rs148405563

rs148405563 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALPL. Location: chromosome 1, position 21,896,823. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ALPLConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 1:21896823
Cytoband: 1p36.12
HGVS: NM_000478.6(ALPL):c.818C>T (p.Thr273Met)
Allele change: Missense_T218M

Associated conditions / phenotypes

Hypophosphatasia

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.