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rs63750092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750092(A;T)
Make rs63750092(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46014277
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750092
ebirs63750092
HLIrs63750092
Exacrs63750092
Varsomers63750092
Maprs63750092
PheGenIrs63750092
hapmaprs63750092
1000 genomesrs63750092
hgdprs63750092
ensemblrs63750092
gopubmedrs63750092
geneviewrs63750092
scholarrs63750092
googlers63750092
pharmgkbrs63750092
gwascentralrs63750092
openSNPrs63750092
23andMers63750092
23andMe allrs63750092
SNP Nexus

SNPshotrs63750092
SNPdbers63750092
MSV3drs63750092
GWAS Ctlgrs63750092
Max Magnitude0
OMIM157140
Desc
Variant0024
Relatedalso


ClinVar
Risk rs63750092(T;T)
Alt rs63750092(T;T)
Reference rs63750092(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.44091643A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015338.26, RCV000084543.1,