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rs63750570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750570(A;A)
Make rs63750570(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position46018629
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750570
ebirs63750570
HLIrs63750570
Exacrs63750570
Varsomers63750570
Maprs63750570
PheGenIrs63750570
hapmaprs63750570
1000 genomesrs63750570
hgdprs63750570
ensemblrs63750570
gopubmedrs63750570
geneviewrs63750570
scholarrs63750570
googlers63750570
pharmgkbrs63750570
gwascentralrs63750570
openSNPrs63750570
23andMers63750570
23andMe allrs63750570
SNP Nexus

SNPshotrs63750570
SNPdbers63750570
MSV3drs63750570
GWAS Ctlgrs63750570
Max Magnitude0
OMIM157140
Desc
Variant0008
Relatedalso


ClinVar
Risk rs63750570(A;A)
Alt rs63750570(A;A)
Reference rs63750570(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.44095995G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015321.25, RCV000084548.1,