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rs137853058

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853058(A;A)
Make rs137853058(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position161973401
GenePARK2
is asnp
is mentioned by
dbSNPrs137853058
ebirs137853058
HLIrs137853058
Exacrs137853058
Varsomers137853058
Maprs137853058
PheGenIrs137853058
hapmaprs137853058
1000 genomesrs137853058
hgdprs137853058
ensemblrs137853058
gopubmedrs137853058
geneviewrs137853058
scholarrs137853058
googlers137853058
pharmgkbrs137853058
gwascentralrs137853058
openSNPrs137853058
23andMers137853058
23andMe allrs137853058
SNP Nexus

SNPshotrs137853058
SNPdbers137853058
MSV3drs137853058
GWAS Ctlgrs137853058
Max Magnitude0
OMIM602544
Desc
Variant0012
Relatedalso
ClinVar
Risk rs137853058(A;A)
Alt rs137853058(A;A)
Reference rs137853058(G;G)
Significance Pathogenic
Disease Parkinson disease 2
Variation info
Gene PARK2
CLNDBN Parkinson disease 2
Reversed 1
HGVS NC_000006.11:g.162394433C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007462.5,