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rs63750756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs63750756(G;G)
Make rs63750756(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46010324
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750756
ebirs63750756
HLIrs63750756
Exacrs63750756
Varsomers63750756
Maprs63750756
PheGenIrs63750756
hapmaprs63750756
1000 genomesrs63750756
hgdprs63750756
ensemblrs63750756
gopubmedrs63750756
geneviewrs63750756
scholarrs63750756
googlers63750756
pharmgkbrs63750756
gwascentralrs63750756
openSNPrs63750756
23andMers63750756
23andMe allrs63750756
SNP Nexus

SNPshotrs63750756
SNPdbers63750756
MSV3drs63750756
GWAS Ctlgrs63750756
Max Magnitude0
OMIM157140
Desc
Variant0009
Relatedalso
ClinVar
Risk rs63750756(G;G)
Alt rs63750756(G;G)
Reference rs63750756(T;T)
Significance Pathogenic
Disease Frontotemporal dementia not provided
Variation info
Gene MAPT
CLNDBN Frontotemporal dementia not provided
Reversed 0
HGVS NC_000017.10:g.44087690T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015322.21, RCV000084521.1,