rs34410987

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs34410987(C;T)

Make rs34410987(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

40283897

Gene

LRRK2

is a	snp
is	mentioned by
dbSNP	rs34410987
dbSNP (classic)	rs34410987
ClinGen	rs34410987
ebi	rs34410987
HLI	rs34410987
Exac	rs34410987
Gnomad	rs34410987
Varsome	rs34410987
LitVar	rs34410987
Map	rs34410987
PheGenI	rs34410987
Biobank	rs34410987
1000 genomes	rs34410987
hgdp	rs34410987
ensembl	rs34410987
geneview	rs34410987
scholar	rs34410987
google	rs34410987
pharmgkb	rs34410987
gwascentral	rs34410987
openSNP	rs34410987
23andMe	rs34410987
SNPshot	rs34410987
SNPdbe	rs34410987
MSV3d	rs34410987
GWAS Ctlg	rs34410987

GMAF

0.001837

Max Magnitude

0

ClinVar
Risk	rs34410987(T;T)
Alt	rs34410987(T;T)
Reference	Rs34410987(C;C)
Significance	Other
Disease	Parkinson disease 8
Variation	info
Gene	LRRK2
CLNDBN	Parkinson disease 8, autosomal dominant
Reversed	0
HGVS	NC_000012.11:g.40677699C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000032422.2,

[PMID 16633828] A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan.