Variant (rsID / SNP)

rs150148567

rs150148567 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WRN. Location: chromosome 8, position 30,948,045. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

WRNConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 8:30948045
Cytoband: 8p12
HGVS: NM_000553.6(WRN):c.1717A>G (p.Thr573Ala)
Allele change: Missense_T573A

Associated conditions / phenotypes

Werner syndrome

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.