Variant (rsID / SNP)

rs140850272

rs140850272 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNCAIP. Location: chromosome 5, position 121,786,959. Clinical significance in the table: Benign.

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Reference-table entries

SNCAIPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:121786959
Cytoband: 5q23.2
HGVS: NM_005460.4(SNCAIP):c.2417G>A (p.Arg806His)
Allele change: Silent

Associated conditions / phenotypes

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.