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rs63750912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750912(C;C)
Make rs63750912(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46010375
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750912
ebirs63750912
HLIrs63750912
Exacrs63750912
Varsomers63750912
Maprs63750912
PheGenIrs63750912
hapmaprs63750912
1000 genomesrs63750912
hgdprs63750912
ensemblrs63750912
gopubmedrs63750912
geneviewrs63750912
scholarrs63750912
googlers63750912
pharmgkbrs63750912
gwascentralrs63750912
openSNPrs63750912
23andMers63750912
23andMe allrs63750912
SNP Nexus

SNPshotrs63750912
SNPdbers63750912
MSV3drs63750912
GWAS Ctlgrs63750912
Max Magnitude0
OMIM157140
Desc
Variant0013
Relatedalso


ClinVar
Risk rs63750912(C;C)
Alt rs63750912(C;C)
Reference rs63750912(T;T)
Significance Pathogenic
Disease Frontotemporal dementia not provided
Variation info
Gene MAPT
CLNDBN Frontotemporal dementia not provided
Reversed 0
HGVS NC_000017.10:g.44087741T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015326.22, RCV000084525.1,