Variant (rsID / SNP)

rs35303786

rs35303786 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRK2. Location: chromosome 12, position 40,713,899. 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: 12:40713899
Cytoband: 12q12
HGVS: NM_198578.4(LRRK2):c.4937T>C (p.Met1646Thr)
Allele change: Missense_M1646T

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.