Rs104893937

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893937(A;A)
Make rs104893937(A;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position176621218
GeneSNCB
is asnp
is mentioned by
dbSNPrs104893937
Exacrs104893937
PheGenIrs104893937
nextbiors104893937
hapmaprs104893937
1000 genomesrs104893937
hgdprs104893937
ensemblrs104893937
gopubmedrs104893937
geneviewrs104893937
scholarrs104893937
googlers104893937
pharmgkbrs104893937
gwascentralrs104893937
openSNPrs104893937
23andMers104893937
23andMe allrs104893937
SNP Nexus

SNPshotrs104893937
SNPdbers104893937
MSV3drs104893937
GMAF0.0009183
OMIM602569
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104893937(A;A)
Alt rs104893937(A;A)
Reference rs104893937(C;C)
Significance Pathogenic
Disease Lewy body dementia
Variation info
Gene SNCB
CLNDBN Lewy body dementia
Reversed 1
HGVS NC_000005.9:g.176048219G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007441.1,