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rs55774500

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs55774500(A;A)
Make rs55774500(A;C)
ReferenceGRCh38 38.1/142
Chromosome6
Position162262692
GenePARK2
is asnp
is mentioned by
dbSNPrs55774500
ebirs55774500
HLIrs55774500
Exacrs55774500
Varsomers55774500
Maprs55774500
PheGenIrs55774500
hapmaprs55774500
1000 genomesrs55774500
hgdprs55774500
ensemblrs55774500
gopubmedrs55774500
geneviewrs55774500
scholarrs55774500
googlers55774500
pharmgkbrs55774500
gwascentralrs55774500
openSNPrs55774500
23andMers55774500
23andMe allrs55774500
SNP Nexus

SNPshotrs55774500
SNPdbers55774500
MSV3drs55774500
GWAS Ctlgrs55774500
GMAF0.001377
Max Magnitude0
OMIM602544
Desc
Variant0011
Relatedalso


ClinVar
Risk rs55774500(A,T;A,T)
Alt rs55774500(A,T;A,T)
Reference rs55774500(C;C)
Significance Other
Disease Parkinson disease 2
Variation info
Gene PARK2
CLNDBN Parkinson disease 2
Reversed 1
HGVS NC_000006.11:g.162683724G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007454.6,