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rs63751048

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751048(C;T)
Make rs63751048(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position87253736
GeneCHMP2B
is asnp
is mentioned by
dbSNPrs63751048
ebirs63751048
HLIrs63751048
Exacrs63751048
Varsomers63751048
Maprs63751048
PheGenIrs63751048
hapmaprs63751048
1000 genomesrs63751048
hgdprs63751048
ensemblrs63751048
gopubmedrs63751048
geneviewrs63751048
scholarrs63751048
googlers63751048
pharmgkbrs63751048
gwascentralrs63751048
openSNPrs63751048
23andMers63751048
23andMe allrs63751048
SNP Nexus

SNPshotrs63751048
SNPdbers63751048
MSV3drs63751048
GWAS Ctlgrs63751048
Max Magnitude0
ClinVar
Risk rs63751048(T;T)
Alt rs63751048(T;T)
Reference rs63751048(C;C)
Significance Pathogenic
Disease Frontotemporal Dementia not provided
Variation info
Gene CHMP2B
CLNDBN Frontotemporal Dementia, Chromosome 3-Linked not provided
Reversed 0
HGVS NC_000003.11:g.87302886C>T
CLNSRC ClinVar GeneReviews Neurodegenerative Brain Diseases Group
CLNACC RCV000020695.1, RCV000084278.1,



[PMID 16954699] Genetic variability in CHMP2B and frontotemporal dementia.