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rs191486604

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs191486604(A;A)
Make rs191486604(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position161350208
GenePARK2
is asnp
is mentioned by
dbSNPrs191486604
dbSNP (old)rs191486604
ClinGenrs191486604
ebirs191486604
HLIrs191486604
Exacrs191486604
Gnomadrs191486604
Varsomers191486604
Maprs191486604
PheGenIrs191486604
Biobankrs191486604
1000 genomesrs191486604
hgdprs191486604
ensemblrs191486604
gopubmedrs191486604
geneviewrs191486604
scholarrs191486604
googlers191486604
pharmgkbrs191486604
gwascentralrs191486604
openSNPrs191486604
23andMers191486604
23andMe allrs191486604
SNPshotrs191486604
SNPdbers191486604
MSV3drs191486604
GWAS Ctlgrs191486604
Max Magnitude0
ClinVar
Risk rs191486604(A;A)
Alt rs191486604(A;A)
Reference Rs191486604(G;G)
Significance Probable-Pathogenic
Disease Parkinson Disease
Variation info
Gene PARK2
CLNDBN Parkinson Disease, Juvenile
Reversed 1
HGVS NC_000006.11:g.161771240C>T
CLNSRC Illumina
CLNACC RCV000269607.1,