Variant (rsID / SNP)

rs183667452

rs183667452 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEB. Location: chromosome 2, position 152,529,136. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NEBUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:152529136
Cytoband: 2q23.3
HGVS: NM_001164508.2(NEB):c.4046T>C (p.Leu1349Pro)
Allele change: Missense_L1349P

Associated conditions / phenotypes

Nemaline myopathy 2

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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