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rs63751392

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0 common genotype
Make rs63751392(-;-)
Make rs63751392(-;AAT)
Make rs63751392(AAT;AAT)
ReferenceGRCh38.p7 38.3/151
Chromosome17
Position46010374
GeneMAPT
is asnp
is mentioned by
dbSNPrs63751392
dbSNP (classic)rs63751392
ClinGenrs63751392
ebirs63751392
HLIrs63751392
Exacrs63751392
Gnomadrs63751392
Varsomers63751392
LitVarrs63751392
Maprs63751392
PheGenIrs63751392
Biobankrs63751392
1000 genomesrs63751392
hgdprs63751392
ensemblrs63751392
geneviewrs63751392
scholarrs63751392
googlers63751392
pharmgkbrs63751392
gwascentralrs63751392
openSNPrs63751392
23andMers63751392
23andMe allrs63751392
SNPshotrs63751392
SNPdbers63751392
MSV3drs63751392
GWAS Ctlgrs63751392
Merged fromRs199422218
Max Magnitude0

aka NM_016835.4(MAPT):c.1838_1840delATA or (p.Asn613del)

OMIM pathogenic variant