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rs1158167

From SNPedia

Orientationplus
Stabilizedplus
Make rs1158167(A;A)
Make rs1158167(A;G)
Make rs1158167(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position23597552
is asnp
is mentioned by
dbSNPrs1158167
ebirs1158167
HLIrs1158167
Exacrs1158167
Varsomers1158167
Maprs1158167
PheGenIrs1158167
hapmaprs1158167
1000 genomesrs1158167
hgdprs1158167
ensemblrs1158167
gopubmedrs1158167
geneviewrs1158167
scholarrs1158167
googlers1158167
pharmgkbrs1158167
gwascentralrs1158167
openSNPrs1158167
23andMers1158167
23andMe allrs1158167
SNP Nexus

SNPshotrs1158167
SNPdbers1158167
MSV3drs1158167
GWAS Ctlgrs1158167
GMAF0.2548
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs1158167
PubMedID [PMID 17903292OA-icon.png]
Condition Cystatin C
Gene CST9L, CST9, CST3
Risk Allele
pValue 9.00E-009
OR NA
95% CI



[PMID 17903291OA-icon.png] The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.


[PMID 17903297OA-icon.png] Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.


GET Evidence
rs1158167
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.6875
summary