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rs62063857

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs62063857(A;G)
Make rs62063857(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position45999299
GeneMAPT, STH
is asnp
is mentioned by
dbSNPrs62063857
ebirs62063857
HLIrs62063857
Exacrs62063857
Varsomers62063857
Maprs62063857
PheGenIrs62063857
hapmaprs62063857
1000 genomesrs62063857
hgdprs62063857
ensemblrs62063857
gopubmedrs62063857
geneviewrs62063857
scholarrs62063857
googlers62063857
pharmgkbrs62063857
gwascentralrs62063857
openSNPrs62063857
23andMers62063857
23andMe allrs62063857
SNP Nexus

SNPshotrs62063857
SNPdbers62063857
MSV3drs62063857
GWAS Ctlgrs62063857
GMAF0.1171
Max Magnitude0

[PMID 19912324OA-icon.png] Association of the MAPT locus with Parkinson's disease


GET Evidence
STH-Q7R
aa_change Gln7Arg
aa_change_short Q7R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.165734
summary



[PMID 25168738] Association of rs62063857 Variant of the Saitohin Gene with Parkinson's Disease