Variant (rsID / SNP)

rs4640000

rs4640000 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRK2. Location: chromosome 12, position 40,699,593. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LRRK2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:40699593
Cytoband: 12q12
HGVS: NM_198578.4(LRRK2):c.3784C>G (p.Pro1262Ala)
Allele change: Missense_P1262A

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.