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rs63750376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750376(G;T)
Make rs63750376(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position45996657
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750376
ebirs63750376
HLIrs63750376
Exacrs63750376
Varsomers63750376
Maprs63750376
PheGenIrs63750376
hapmaprs63750376
1000 genomesrs63750376
hgdprs63750376
ensemblrs63750376
gopubmedrs63750376
geneviewrs63750376
scholarrs63750376
googlers63750376
pharmgkbrs63750376
gwascentralrs63750376
openSNPrs63750376
23andMers63750376
23andMe allrs63750376
SNP Nexus

SNPshotrs63750376
SNPdbers63750376
MSV3drs63750376
GWAS Ctlgrs63750376
Max Magnitude0
OMIM157140
Desc
Variant0002
Relatedalso


ClinVar
Risk rs63750376(T;T)
Alt rs63750376(T;T)
Reference rs63750376(G;G)
Significance Pathogenic
Disease Frontotemporal dementia not provided
Variation info
Gene MAPT
CLNDBN Frontotemporal dementia not provided
Reversed 0
HGVS NC_000017.10:g.44074023G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015315.26, RCV000084519.1,