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rs137853056

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853056(A;A)
Make rs137853056(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position161350139
GenePARK2
is asnp
is mentioned by
dbSNPrs137853056
ebirs137853056
HLIrs137853056
Exacrs137853056
Varsomers137853056
Maprs137853056
PheGenIrs137853056
hapmaprs137853056
1000 genomesrs137853056
hgdprs137853056
ensemblrs137853056
gopubmedrs137853056
geneviewrs137853056
scholarrs137853056
googlers137853056
pharmgkbrs137853056
gwascentralrs137853056
openSNPrs137853056
23andMers137853056
23andMe allrs137853056
SNP Nexus

SNPshotrs137853056
SNPdbers137853056
MSV3drs137853056
GWAS Ctlgrs137853056
Max Magnitude0
OMIM602544
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137853056(A;A)
Alt rs137853056(A;A)
Reference rs137853056(G;G)
Significance Pathogenic
Disease Parkinson disease 2
Variation info
Gene PARK2
CLNDBN Parkinson disease 2
Reversed 1
HGVS NC_000006.11:g.161771171C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007458.3,