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rs7308720

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7308720(C;G)
Make rs7308720(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position40263898
GeneLRRK2
is asnp
is mentioned by
dbSNPrs7308720
ebirs7308720
HLIrs7308720
Exacrs7308720
Varsomers7308720
Maprs7308720
PheGenIrs7308720
hapmaprs7308720
1000 genomesrs7308720
hgdprs7308720
ensemblrs7308720
gopubmedrs7308720
geneviewrs7308720
scholarrs7308720
googlers7308720
pharmgkbrs7308720
gwascentralrs7308720
openSNPrs7308720
23andMers7308720
23andMe allrs7308720
SNP Nexus

SNPshotrs7308720
SNPdbers7308720
MSV3drs7308720
GWAS Ctlgrs7308720
GMAF0.1015
Max Magnitude0
? (C;C) (C;G) (G;G) 28
OMIM609007
DescLEUCINE-RICH REPEAT KINASE 2; LRRK2
Variant
Relatedalso

[PMID 20186690] Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study.


GET Evidence
LRRK2-N551K
aa_change Asn551Lys
aa_change_short N551K
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0955923
summary



ClinVar
Risk rs7308720(G;G)
Alt rs7308720(G;G)
Reference rs7308720(C;C)
Significance Unknown
Disease Parkinson disease 8
Variation info
Gene LRRK2
CLNDBN Parkinson disease 8, autosomal dominant
Reversed 0
HGVS NC_000012.11:g.40657700C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000032413.1,