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rs104893878

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893878(C;C)
Make rs104893878(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position89835580
GeneFGF22, SNCA
is asnp
is mentioned by
dbSNPrs104893878
ebirs104893878
HLIrs104893878
Exacrs104893878
Varsomers104893878
Maprs104893878
PheGenIrs104893878
hapmaprs104893878
1000 genomesrs104893878
hgdprs104893878
ensemblrs104893878
gopubmedrs104893878
geneviewrs104893878
scholarrs104893878
googlers104893878
pharmgkbrs104893878
gwascentralrs104893878
openSNPrs104893878
23andMers104893878
23andMe allrs104893878
SNP Nexus

SNPshotrs104893878
SNPdbers104893878
MSV3drs104893878
GWAS Ctlgrs104893878
Max Magnitude0
OMIM163890
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104893878(C;C)
Alt rs104893878(C;C)
Reference rs104893878(G;G)
Significance Pathogenic
Disease Parkinson disease 1
Variation info
Gene SNCA-AS1 SNCA
CLNDBN Parkinson disease 1
Reversed 1
HGVS NC_000004.11:g.90756731C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015045.27,