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rs63751438

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751438(C;T)
Make rs63751438(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46010388
GeneMAPT
is asnp
is mentioned by
dbSNPrs63751438
ebirs63751438
HLIrs63751438
Exacrs63751438
Varsomers63751438
Maprs63751438
PheGenIrs63751438
hapmaprs63751438
1000 genomesrs63751438
hgdprs63751438
ensemblrs63751438
gopubmedrs63751438
geneviewrs63751438
scholarrs63751438
googlers63751438
pharmgkbrs63751438
gwascentralrs63751438
openSNPrs63751438
23andMers63751438
23andMe allrs63751438
SNP Nexus

SNPshotrs63751438
SNPdbers63751438
MSV3drs63751438
GWAS Ctlgrs63751438
Max Magnitude0
OMIM157140
Desc
Variant0012
Relatedalso
ClinVar
Risk rs63751438(T;T)
Alt rs63751438(T;T)
Reference rs63751438(C;C)
Significance Pathogenic
Disease Frontotemporal dementia not provided
Variation info
Gene MAPT
CLNDBN Frontotemporal dementia not provided
Reversed 0
HGVS NC_000017.10:g.44087754C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015325.22, RCV000084526.1,