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rs104893877

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893877(A;A)
Make rs104893877(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position89828149
GeneSNCA
is asnp
is mentioned by
dbSNPrs104893877
ebirs104893877
HLIrs104893877
Exacrs104893877
Varsomers104893877
Maprs104893877
PheGenIrs104893877
hapmaprs104893877
1000 genomesrs104893877
hgdprs104893877
ensemblrs104893877
gopubmedrs104893877
geneviewrs104893877
scholarrs104893877
googlers104893877
pharmgkbrs104893877
gwascentralrs104893877
openSNPrs104893877
23andMers104893877
23andMe allrs104893877
SNP Nexus

SNPshotrs104893877
SNPdbers104893877
MSV3drs104893877
GWAS Ctlgrs104893877
Max Magnitude0
OMIM163890
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893877(A;A)
Alt rs104893877(A;A)
Reference rs104893877(G;G)
Significance Pathogenic
Disease Parkinson disease 1
Variation info
Gene SNCA
CLNDBN Parkinson disease 1
Reversed 1
HGVS NC_000004.11:g.90749300C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015044.25,