Variant (rsID / SNP)

rs80358366

rs80358366 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NIPBL. Location: chromosome 5, position 37,022,374. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

NIPBLLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 5:37022374
Cytoband: 5p13.2
HGVS: NM_133433.4(NIPBL):c.5456G>A (p.Arg1819Gln)
Allele change: Missense_R1819Q

Associated conditions / phenotypes

Cornelia de Lange syndrome 1

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.