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rs137853054

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853054(C;G)
Make rs137853054(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position161973317
GenePARK2
is asnp
is mentioned by
dbSNPrs137853054
ebirs137853054
HLIrs137853054
Exacrs137853054
Varsomers137853054
Maprs137853054
PheGenIrs137853054
hapmaprs137853054
1000 genomesrs137853054
hgdprs137853054
ensemblrs137853054
gopubmedrs137853054
geneviewrs137853054
scholarrs137853054
googlers137853054
pharmgkbrs137853054
gwascentralrs137853054
openSNPrs137853054
23andMers137853054
23andMe allrs137853054
SNP Nexus

SNPshotrs137853054
SNPdbers137853054
MSV3drs137853054
GWAS Ctlgrs137853054
Max Magnitude0
OMIM602544
Desc
Variant0003
Relatedalso
OMIM602544
Desc
Variant0021
Relatedalso
ClinVar
Risk rs137853054(A,G,T;A,G,T)
Alt rs137853054(A,G,T;A,G,T)
Reference rs137853054(C;C)
Significance Pathogenic
Disease Parkinson disease 2
Variation info
Gene PARK2
CLNDBN Parkinson disease 2
Reversed 1
HGVS NC_000006.11:g.162394349G>A; NC_000006.11:g.162394349G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007470.4, RCV000007452.5,