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rs78365431

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs78365431(G;T)
Make rs78365431(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position40298479
GeneLRRK2
is asnp
is mentioned by
dbSNPrs78365431
ebirs78365431
HLIrs78365431
Exacrs78365431
Varsomers78365431
Maprs78365431
PheGenIrs78365431
hapmaprs78365431
1000 genomesrs78365431
hgdprs78365431
ensemblrs78365431
gopubmedrs78365431
geneviewrs78365431
scholarrs78365431
googlers78365431
pharmgkbrs78365431
gwascentralrs78365431
openSNPrs78365431
23andMers78365431
23andMe allrs78365431
SNP Nexus

SNPshotrs78365431
SNPdbers78365431
MSV3drs78365431
GWAS Ctlgrs78365431
GMAF0.002755
Max Magnitude0

[PMID 21632271OA-icon.png] Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin America

ClinVar
Risk rs78365431(T;T)
Alt rs78365431(T;T)
Reference rs78365431(G;G)
Significance Unknown
Disease Parkinson disease 8
Variation info
Gene LRRK2
CLNDBN Parkinson disease 8, autosomal dominant
Reversed 0
HGVS NC_000012.11:g.40692281G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032437.1,