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Variant (rsID / SNP)

rs104894293

RAPSN

rs104894293 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAPSN. Location: chromosome 11, position 47,463,227. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

RAPSNConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:47463227
Cytoband
11p11.2
HGVS
NM_005055.5(RAPSN):c.848T>C (p.Leu283Pro)
Allele change
Silent

Associated conditions / phenotypes

Congenital myasthenic syndrome 11|Fetal akinesia deformation sequence 1|Global developmental delay|RAPSN-Related Disorders

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.