Variant (rsID / SNP)

rs145946864

rs145946864 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARSL. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ARSLConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xp22.33
HGVS: NM_000047.3(ARSL):c.337C>T (p.Leu113Phe)
Allele change: Missense_L68F

Associated conditions / phenotypes

X-linked chondrodysplasia punctata 1

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.