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rs63751264

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751264(A;T)
Make rs63751264(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46018726
GeneMAPT
is asnp
is mentioned by
dbSNPrs63751264
ebirs63751264
HLIrs63751264
Exacrs63751264
Varsomers63751264
Maprs63751264
PheGenIrs63751264
hapmaprs63751264
1000 genomesrs63751264
hgdprs63751264
ensemblrs63751264
gopubmedrs63751264
geneviewrs63751264
scholarrs63751264
googlers63751264
pharmgkbrs63751264
gwascentralrs63751264
openSNPrs63751264
23andMers63751264
23andMe allrs63751264
SNP Nexus

SNPshotrs63751264
SNPdbers63751264
MSV3drs63751264
GWAS Ctlgrs63751264
Max Magnitude0
OMIM157140
DescPick's disease
Variant0016
Relatedalso


ClinVar
Risk rs63751264(T;T)
Alt rs63751264(T;T)
Reference rs63751264(A;A)
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.44096092A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015329.21, RCV000084552.1,