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rs104893875

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893875(A;A)
Make rs104893875(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position89828170
GeneSNCA
is asnp
is mentioned by
dbSNPrs104893875
ebirs104893875
HLIrs104893875
Exacrs104893875
Varsomers104893875
Maprs104893875
PheGenIrs104893875
hapmaprs104893875
1000 genomesrs104893875
hgdprs104893875
ensemblrs104893875
gopubmedrs104893875
geneviewrs104893875
scholarrs104893875
googlers104893875
pharmgkbrs104893875
gwascentralrs104893875
openSNPrs104893875
23andMers104893875
23andMe allrs104893875
SNP Nexus

SNPshotrs104893875
SNPdbers104893875
MSV3drs104893875
GWAS Ctlgrs104893875
Max Magnitude0
OMIM163890
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104893875(A;A)
Alt rs104893875(A;A)
Reference rs104893875(G;G)
Significance Pathogenic
Disease Lewy body dementia
Variation info
Gene SNCA
CLNDBN Lewy body dementia
Reversed 1
HGVS NC_000004.11:g.90749321C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015047.25,



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