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rs63750869

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750869(A;A)
Make rs63750869(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position46018707
GeneMAPT
is asnp
is mentioned by
dbSNPrs63750869
dbSNP (classic)rs63750869
ClinGenrs63750869
ebirs63750869
HLIrs63750869
Exacrs63750869
Gnomadrs63750869
Varsomers63750869
LitVarrs63750869
Maprs63750869
PheGenIrs63750869
Biobankrs63750869
1000 genomesrs63750869
hgdprs63750869
ensemblrs63750869
geneviewrs63750869
scholarrs63750869
googlers63750869
pharmgkbrs63750869
gwascentralrs63750869
openSNPrs63750869
23andMers63750869
23andMe allrs63750869
SNPshotrs63750869
SNPdbers63750869
MSV3drs63750869
GWAS Ctlgrs63750869
Max Magnitude0
ClinVar
Risk rs63750869(A;A)
Alt rs63750869(A;A)
Reference Rs63750869(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAPT
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.44096073G>A
CLNSRC
CLNACC RCV000084551.1,