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rs63750424

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750424(C;T)
Make rs63750424(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46024061
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750424
ebirs63750424
HLIrs63750424
Exacrs63750424
Varsomers63750424
Maprs63750424
PheGenIrs63750424
hapmaprs63750424
1000 genomesrs63750424
hgdprs63750424
ensemblrs63750424
gopubmedrs63750424
geneviewrs63750424
scholarrs63750424
googlers63750424
pharmgkbrs63750424
gwascentralrs63750424
openSNPrs63750424
23andMers63750424
23andMe allrs63750424
SNP Nexus

SNPshotrs63750424
SNPdbers63750424
MSV3drs63750424
GWAS Ctlgrs63750424
Max Magnitude0
OMIM157140
Desc
Variant0003
Relatedalso


ClinVar
Risk rs63750424(T;T)
Alt rs63750424(T;T)
Reference rs63750424(C;C)
Significance Pathogenic
Disease Frontotemporal dementia not provided
Variation info
Gene MAPT
CLNDBN Frontotemporal dementia not provided
Reversed 0
HGVS NC_000017.10:g.44101427C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015316.26, RCV000084554.1,