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Rs104893936

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893936(A;A)
Make rs104893936(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position176626472
GeneSNCB
is asnp
is mentioned by
dbSNPrs104893936
PheGenIrs104893936
nextbiors104893936
hapmaprs104893936
1000 genomesrs104893936
hgdprs104893936
ensemblrs104893936
gopubmedrs104893936
geneviewrs104893936
scholarrs104893936
googlers104893936
pharmgkbrs104893936
gwascentralrs104893936
openSNPrs104893936
23andMers104893936
23andMe allrs104893936
SNP Nexus

SNPshotrs104893936
SNPdbers104893936
MSV3drs104893936
Max Magnitude0
OMIM602569
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893936(A;A)
Alt rs104893936(A;A)
Reference rs104893936(G;G)
Significance Pathogenic
Disease Lewy body dementia
Variation info
Gene SNCB
CLNDBN Lewy body dementia
Reversed 1
HGVS NC_000005.9:g.176053473C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007440.1,