Variant (rsID / SNP)

rs138958687

rs138958687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP7A. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ATP7AConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xq21.1
HGVS: NM_000052.7(ATP7A):c.2903A>G (p.Glu968Gly)
Allele change: Missense_E890G

Associated conditions / phenotypes

Menkes kinky-hair syndrome|X-linked distal spinal muscular atrophy type 3|Cutis laxa, X-linked|Menkes kinky-hair syndrome|Ehlers-Danlos 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.