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Variant (rsID / SNP)

rs367626762

NEB

rs367626762 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEB. Location: chromosome 2, position 152,384,038. 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
2:152384038
Cytoband
2q23.3
HGVS
NM_001164508.2(NEB):c.21797C>T (p.Pro7266Leu)
Allele change
Missense_P7266L

Associated conditions / phenotypes

Peripheral neuropathy|Nemaline myopathy 2|Actin accumulation myopathy

Public references

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