Variant (rsID / SNP)

rs79909111

rs79909111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRK2. Location: chromosome 12, position 40,714,983. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

LRRK2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:40714983
Cytoband: 12q12
HGVS: NM_198578.4(LRRK2):c.5163A>G (p.Ser1721=)
Allele change: Synonymous_S1721S

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.