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Variant (rsID / SNP)

rs201822024

NEBL

rs201822024 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEBL. Location: chromosome 10, position 21,102,862. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NEBLConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:21102862
Cytoband
10p12.31
HGVS
NM_006393.3(NEBL):c.2346+6G>A
Allele change
Silent

Associated conditions / phenotypes

Primary dilated cardiomyopathy

Public references

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