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rs63750512

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750512(A;A)
Make rs63750512(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position46024010
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750512
ebirs63750512
HLIrs63750512
Exacrs63750512
Varsomers63750512
Maprs63750512
PheGenIrs63750512
hapmaprs63750512
1000 genomesrs63750512
hgdprs63750512
ensemblrs63750512
gopubmedrs63750512
geneviewrs63750512
scholarrs63750512
googlers63750512
pharmgkbrs63750512
gwascentralrs63750512
openSNPrs63750512
23andMers63750512
23andMe allrs63750512
SNP Nexus

SNPshotrs63750512
SNPdbers63750512
MSV3drs63750512
GWAS Ctlgrs63750512
Max Magnitude0
OMIM157140
DescPick's disease
Variant0011
Relatedalso
ClinVar
Risk rs63750512(A,C;A,C)
Alt rs63750512(A,C;A,C)
Reference rs63750512(G;G)
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.44101376G>A; NC_000017.10:g.44101376G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015324.26, RCV000084553.1,