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Variant (rsID / SNP)

rs117861109

NEB

rs117861109 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEB. Location: chromosome 2, position 152,342,288. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NEBConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:152342288
Cytoband
2q23.3
HGVS
NM_001164508.2(NEB):c.25564G>A (p.Val8522Ile)
Allele change
Missense_V8522I

Associated conditions / phenotypes

Nemaline myopathy 2

Public references

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