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rs9468

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9468(C;C)
Make rs9468(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46024197
GeneMAPT
is asnp
is mentioned by
dbSNPrs9468
dbSNP (old)rs9468
ClinGenrs9468
ebirs9468
HLIrs9468
Exacrs9468
Gnomadrs9468
Varsomers9468
Maprs9468
PheGenIrs9468
Biobankrs9468
1000 genomesrs9468
hgdprs9468
ensemblrs9468
gopubmedrs9468
geneviewrs9468
scholarrs9468
googlers9468
pharmgkbrs9468
gwascentralrs9468
openSNPrs9468
23andMers9468
23andMe allrs9468
SNP Nexus

SNPshotrs9468
SNPdbers9468
MSV3drs9468
GWAS Ctlgrs9468
GMAF0.1157
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 22104010OA-icon.png] SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population


[PMID 22027014OA-icon.png] The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease


[PMID 17267408OA-icon.png] Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.


[PMID 19761364OA-icon.png] Predicting response to short-acting bronchodilator medication using Bayesian networks.


[PMID 20116045OA-icon.png] The distribution and most recent common ancestor of the 17q21 inversion in humans.


ClinVar
Risk rs9468(C;C)
Alt rs9468(C;C)
Reference Rs9468(T;T)
Significance Non-pathogenic
Disease MAPT-Related Spectrum Disorders
Variation info
Gene MAPT
CLNDBN MAPT-Related Spectrum Disorders
Reversed 0
HGVS NC_000017.10:g.44101563T>C
CLNSRC
CLNACC RCV000399955.1,