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

rs1341667

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1341667(A;G)
Make rs1341667(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position68882104
GeneSTOX1
is asnp
is mentioned by
dbSNPrs1341667
ebirs1341667
HLIrs1341667
Exacrs1341667
Varsomers1341667
Maprs1341667
PheGenIrs1341667
hapmaprs1341667
1000 genomesrs1341667
hgdprs1341667
ensemblrs1341667
gopubmedrs1341667
geneviewrs1341667
scholarrs1341667
googlers1341667
pharmgkbrs1341667
gwascentralrs1341667
openSNPrs1341667
23andMers1341667
23andMe allrs1341667
SNP Nexus

SNPshotrs1341667
SNPdbers1341667
MSV3drs1341667
GWAS Ctlgrs1341667
GMAF0.3673
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM609397
Desc
Variant0001
Relatedalso


ClinVar
Risk rs1341667(G;G)
Alt rs1341667(G;G)
Reference rs1341667(A;A)
Significance Other
Disease Preeclampsia/eclampsia 4
Variation info
Gene STOX1
CLNDBN Preeclampsia/eclampsia 4
Reversed 1
HGVS NC_000010.10:g.70641860T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001789.1,



[PMID 16385451OA-icon.png] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.


GET Evidence
STOX1-Y43H
aa_change Tyr43His
aa_change_short Y43H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.572086
summary