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PYCR2 rs876657403: what the research says

rs876657403
Carrier Status
Limited evidenceGene: PYCR2

This pathogenic variant is linked to hypomyelinating leukodystrophy 10, a severe neurological condition.

Rare

Our full long-form research profile for rs876657403 — genotype interpretations, evidence review, and FAQ — is being written and will appear on this page soon.
dbSNP ClinVar GWAS Catalog Google Scholar

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