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Variant (rsID / SNP)

rs146616621

NEB

rs146616621 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEB. Location: chromosome 2, position 152,534,260. 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
2:152534260
Cytoband
2q23.3
HGVS
NM_001164508.2(NEB):c.3593A>G (p.Asn1198Ser)
Allele change
Missense_N1198S

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.