Variant (rsID / SNP)

rs786204455

rs786204455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPC1. Location: chromosome 18, position 21,116,707. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

NPC1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 18:21116707
Cytoband: 18q11.2
HGVS: NM_000271.5(NPC1):c.3175C>T (p.Arg1059Ter)
Allele change: Nonsense_R1059X

Associated conditions / phenotypes

Niemann-Pick disease, type C1|Niemann-Pick disease, type C

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.