Have questions? Visit https://www.reddit.com/r/SNPedia

rs199422218

From SNPedia

Merged intors63751392
Orientationplus
Stabilizedplus
Geno Mag Summary
(AAT;AAT) 0 common in clinvar
Make rs199422218(-;-)
Make rs199422218(-;AAT)
ReferenceGRCh38 38.1/141
Chromosome17
Position46010373
GeneMAPT
is asnp
is mentioned by
dbSNPrs199422218
dbSNP (old)rs199422218
ClinGenrs199422218
ebirs199422218
HLIrs199422218
Exacrs199422218
Gnomadrs199422218
Varsomers199422218
Maprs199422218
PheGenIrs199422218
Biobankrs199422218
1000 genomesrs199422218
hgdprs199422218
ensemblrs199422218
gopubmedrs199422218
geneviewrs199422218
scholarrs199422218
googlers199422218
pharmgkbrs199422218
gwascentralrs199422218
openSNPrs199422218
23andMers199422218
23andMe allrs199422218
SNP Nexus

SNPshotrs199422218
SNPdbers199422218
MSV3drs199422218
GWAS Ctlgrs199422218
StatusMerged into rs63751392
Max Magnitude0
ClinVar
Risk
Alt
Reference rs199422218(ATA;ATA)
Significance Other
Disease Supranuclear palsy Parkinson disease not provided
Variation info
Gene MAPT
CLNDBN Supranuclear palsy, progressive, 1, atypical Parkinson disease, late-onset not provided
Reversed 0
HGVS NC_000017.10:g.44087740_44087742delATA
CLNSRC OMIM Allelic Variant
CLNACC RCV000015334.26, RCV000015335.3, RCV000084581.1,