Variant (rsID / SNP)

rs61742278

rs61742278 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP7A. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ATP7ABenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Cytoband: Xq21.1
HGVS: NM_000052.7(ATP7A):c.1823A>G (p.Tyr608Cys)
Allele change: Missense_Y608C

Associated conditions / phenotypes

X-linked distal spinal muscular atrophy type 3|Cutis laxa, X-linked|Menkes kinky-hair syndrome|History of neurodevelopmental disorder|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.