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rs1060499619

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499619(C;C)
Make rs1060499619(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position32681590
GeneSYNJ1
is asnp
is mentioned by
dbSNPrs1060499619
dbSNP (old)rs1060499619
ClinGenrs1060499619
ebirs1060499619
HLIrs1060499619
Exacrs1060499619
Gnomadrs1060499619
Varsomers1060499619
Maprs1060499619
PheGenIrs1060499619
Biobankrs1060499619
1000 genomesrs1060499619
hgdprs1060499619
ensemblrs1060499619
gopubmedrs1060499619
geneviewrs1060499619
scholarrs1060499619
googlers1060499619
pharmgkbrs1060499619
gwascentralrs1060499619
openSNPrs1060499619
23andMers1060499619
23andMe allrs1060499619
SNPshotrs1060499619
SNPdbers1060499619
MSV3drs1060499619
GWAS Ctlgrs1060499619
Max Magnitude0
ClinVar
Risk rs1060499619(C;C)
Alt rs1060499619(C;C)
Reference Rs1060499619(G;G)
Significance Pathogenic
Disease Parkinson disease 20
Variation info
Gene SYNJ1
CLNDBN Parkinson disease 20, early-onset
Reversed 1
HGVS NC_000021.8:g.34053900C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000445361.1,