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rs63750972

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750972(C;T)
Make rs63750972(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46010416
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750972
ebirs63750972
HLIrs63750972
Exacrs63750972
Varsomers63750972
Maprs63750972
PheGenIrs63750972
hapmaprs63750972
1000 genomesrs63750972
hgdprs63750972
ensemblrs63750972
gopubmedrs63750972
geneviewrs63750972
scholarrs63750972
googlers63750972
pharmgkbrs63750972
gwascentralrs63750972
openSNPrs63750972
23andMers63750972
23andMe allrs63750972
SNP Nexus

SNPshotrs63750972
SNPdbers63750972
MSV3drs63750972
GWAS Ctlgrs63750972
Max Magnitude0
ClinVar
Risk rs63750972(T;T)
Alt rs63750972(T;T)
Reference rs63750972(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.44087782C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015317.25, RCV000084536.1,