RS34778348 LRRK2

Health Risk Chr 12:40363526
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What This Variant Does
"In perfect contrast to another SNP also within the LRRK2 gene, rs34637584, this SNP, rs34778348, is ...
Associated Conditions
Autosomal dominant Parkinson disease 8
Parkinson disease
Autosomal dominant Parkinson disease 8
Parkinson disease
GWAS Studies (4)
Trait Risk Allele OR / Beta P-value Study
Parkinson's disease C OR: 0.61 3E-30 PubMed
Parkinson's disease — OR: 2.23 3E-21 PubMed
Parkinson's disease A OR: 2.56 5E-13 PubMed
Parkinson's disease A OR: 3.53 2E-9 PubMed
Other Variants in LRRK2
rs33939927 rs35801418 rs34805604 rs34637584 rs35870237 rs34995376 rs78501232 rs35328937 rs7308720 rs35173587
Ask Dr. Hemsworth about this variant