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rs66737902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs66737902(C;C)
Make rs66737902(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position40367861
GeneLOC105369736, LRRK2
is asnp
is mentioned by
dbSNPrs66737902
dbSNP (old)rs66737902
ClinGenrs66737902
ebirs66737902
HLIrs66737902
Exacrs66737902
Varsomers66737902
Maprs66737902
PheGenIrs66737902
Biobankrs66737902
1000 genomesrs66737902
hgdprs66737902
ensemblrs66737902
gopubmedrs66737902
geneviewrs66737902
scholarrs66737902
googlers66737902
pharmgkbrs66737902
gwascentralrs66737902
openSNPrs66737902
23andMers66737902
23andMe allrs66737902
SNP Nexus

SNPshotrs66737902
SNPdbers66737902
MSV3drs66737902
GWAS Ctlgrs66737902
Max Magnitude0

[PMID 24758914] The screening of the 3'UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson's disease


ClinVar
Risk rs66737902(C;C)
Alt rs66737902(C;C)
Reference Rs66737902(T;T)
Significance Probable-non-pathogenic
Disease Parkinson disease 8
Variation info
Gene LRRK2
CLNDBN Parkinson disease 8, autosomal dominant
Reversed 0
HGVS NC_000012.11:g.40761663T>C
CLNSRC
CLNACC RCV000371980.1,