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rs63750711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750711(A;T)
Make rs63750711(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46018645
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750711
ebirs63750711
HLIrs63750711
Exacrs63750711
Varsomers63750711
Maprs63750711
PheGenIrs63750711
hapmaprs63750711
1000 genomesrs63750711
hgdprs63750711
ensemblrs63750711
gopubmedrs63750711
geneviewrs63750711
scholarrs63750711
googlers63750711
pharmgkbrs63750711
gwascentralrs63750711
openSNPrs63750711
23andMers63750711
23andMe allrs63750711
SNP Nexus

SNPshotrs63750711
SNPdbers63750711
MSV3drs63750711
GWAS Ctlgrs63750711
Max Magnitude0
OMIM157140
Desc
Variant0014
Relatedalso


ClinVar
Risk rs63750711(T;T)
Alt rs63750711(T;T)
Reference rs63750711(A;A)
Significance Pathogenic
Disease Frontotemporal dementia not provided
Variation info
Gene MAPT
CLNDBN Frontotemporal dementia not provided
Reversed 0
HGVS NC_000017.10:g.44096011A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015327.27, RCV000084549.1,