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rs63750355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750355(C;T)
Make rs63750355(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position87253472
GeneCHMP2B
is asnp
is mentioned by
dbSNPrs63750355
ebirs63750355
HLIrs63750355
Exacrs63750355
Varsomers63750355
Maprs63750355
PheGenIrs63750355
hapmaprs63750355
1000 genomesrs63750355
hgdprs63750355
ensemblrs63750355
gopubmedrs63750355
geneviewrs63750355
scholarrs63750355
googlers63750355
pharmgkbrs63750355
gwascentralrs63750355
openSNPrs63750355
23andMers63750355
23andMe allrs63750355
SNP Nexus

SNPshotrs63750355
SNPdbers63750355
MSV3drs63750355
GWAS Ctlgrs63750355
Max Magnitude0
OMIM609512
Desc
Variant0004
Relatedalso


ClinVar
Risk rs63750355(T;T)
Alt rs63750355(T;T)
Reference rs63750355(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.87302622C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001722.2, RCV000084276.1,