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rs6413453

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs6413453(C;T)
Make rs6413453(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161222526
GeneAPOA2
is asnp
is mentioned by
dbSNPrs6413453
dbSNP (old)rs6413453
ClinGenrs6413453
ebirs6413453
HLIrs6413453
Exacrs6413453
Gnomadrs6413453
Varsomers6413453
Maprs6413453
PheGenIrs6413453
Biobankrs6413453
1000 genomesrs6413453
hgdprs6413453
ensemblrs6413453
gopubmedrs6413453
geneviewrs6413453
scholarrs6413453
googlers6413453
pharmgkbrs6413453
gwascentralrs6413453
openSNPrs6413453
23andMers6413453
23andMe allrs6413453
SNP Nexus

SNPshotrs6413453
SNPdbers6413453
MSV3drs6413453
GWAS Ctlgrs6413453
GMAF0.1074
Max Magnitude0
? (C;C) (C;T) (T;T) 28
A meta-analysis of several APOA2 SNPs (including this one) found no association between any APOA2 SNPs studied and type-2 diabetes.[PMID 19216768OA-icon.png]


[PMID 18269685] Type 2 diabetes susceptibility genes on chromosome 1q21-24.


[PMID 26590203OA-icon.png] Identification of Sequence Variation in the Apolipoprotein A2 Gene and Their Relationship with Serum High-Density Lipoprotein Cholesterol Levels


ClinVar
Risk rs6413453(T;T)
Alt rs6413453(T;T)
Reference Rs6413453(C;C)
Significance Probable-non-pathogenic
Disease Apolipoprotein A-II deficiency
Variation info
Gene APOA2
CLNDBN Apolipoprotein A-II deficiency
Reversed 1
HGVS NC_000001.10:g.161192316G>A
CLNSRC
CLNACC RCV000380848.1,