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Variant (rsID / SNP)

rs61876771

SMPD1

rs61876771 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMPD1. Location: chromosome 11, position 6,413,108. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SMPD1Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
11:6413108
Cytoband
11p15.4
HGVS
NM_000543.5(SMPD1):c.813T>C (p.Pro271=)
Allele change
Synonymous_P271P

Associated conditions / phenotypes

Niemann-Pick disease, type A|Niemann-Pick disease, type B|Niemann-Pick disease, type A|Sphingomyelin/cholesterol lipidosis

Public references

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