Variant (rsID / SNP)

rs141243713

rs141243713 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPC1. Location: chromosome 18, position 21,141,474. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NPC1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 18:21141474
Cytoband: 18q11.2
HGVS: NM_000271.5(NPC1):c.481C>T (p.Arg161Trp)
Allele change: Missense_R161W

Associated conditions / phenotypes

Niemann-Pick disease, type C1

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.