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rs63750635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750635(C;T)
Make rs63750635(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46014286
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750635
ebirs63750635
HLIrs63750635
Exacrs63750635
Varsomers63750635
Maprs63750635
PheGenIrs63750635
hapmaprs63750635
1000 genomesrs63750635
hgdprs63750635
ensemblrs63750635
gopubmedrs63750635
geneviewrs63750635
scholarrs63750635
googlers63750635
pharmgkbrs63750635
gwascentralrs63750635
openSNPrs63750635
23andMers63750635
23andMe allrs63750635
SNP Nexus

SNPshotrs63750635
SNPdbers63750635
MSV3drs63750635
GWAS Ctlgrs63750635
Max Magnitude0
OMIM157140
DescPick's disease
Variant0018
Relatedalso


ClinVar
Risk rs63750635(T;T)
Alt rs63750635(T;T)
Reference rs63750635(C;C)
Significance Pathogenic
Disease Pick's disease not provided
Variation info
Gene MAPT
CLNDBN Pick's disease not provided
Reversed 0
HGVS NC_000017.10:g.44091652C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015331.26, RCV000084544.1,