Variant (rsID / SNP)

rs10878371

rs10878371 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRK2. Location: chromosome 12, position 40,716,260. Clinical significance in the table: Benign.

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Reference-table entries

LRRK2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:40716260
Cytoband: 12q12
HGVS: NM_198578.4(LRRK2):c.5457T>C (p.Gly1819=)
Allele change: Synonymous_G1819G

Associated conditions / phenotypes

Autosomal dominant Parkinson disease 8

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.