Variant (rsID / SNP)

rs28937592

rs28937592 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNCAIP. Location: chromosome 5, position 121,786,403. Clinical significance in the table: Likely benign.

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Reference-table entries

SNCAIPLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:121786403
Cytoband: 5q23.2
HGVS: NM_005460.4(SNCAIP):c.1861C>T (p.Arg621Cys)
Allele change: Silent

Associated conditions / phenotypes

Parkinson disease, late-onset|Parkinson Disease, Dominant/Recessive

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.