Variant (rsID / SNP)

rs374628199

rs374628199 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP7B. Location: chromosome 13, position 52,511,799. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ATP7BConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 13:52511799
Cytoband: 13q14.3
HGVS: NM_000053.4(ATP7B):c.3716T>G (p.Val1239Gly)
Allele change: Missense_V1155G

Associated conditions / phenotypes

Wilson disease

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.