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rs714052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs714052(C;C)
Make rs714052(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position73450539
GeneBAZ1B
is asnp
is mentioned by
dbSNPrs714052
ebirs714052
HLIrs714052
Exacrs714052
Varsomers714052
Maprs714052
PheGenIrs714052
hapmaprs714052
1000 genomesrs714052
hgdprs714052
ensemblrs714052
gopubmedrs714052
geneviewrs714052
scholarrs714052
googlers714052
pharmgkbrs714052
gwascentralrs714052
openSNPrs714052
23andMers714052
23andMe allrs714052
SNP Nexus

SNPshotrs714052
SNPdbers714052
MSV3drs714052
GWAS Ctlgrs714052
GMAF0.08815
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19060906OA-icon.png]
Trait Triglycerides
Title Common variants at 30 loci contribute to polygenic dyslipidemia
Risk Allele G
P-val 3E-15
Odds Ratio 0.16 [0.10-0.22] SD decrease


GWAS snp
PMID [PMID 20657596OA-icon.png]
Trait Hypertriglyceridemia
Title Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
Risk Allele
P-val 0.000003
Odds Ratio 2.27 [1.61-3.23]


GET Evidence
rs714052
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.101562
summary



GWAS snp
PMID [PMID 20139978]
Trait Triglycerides
Title Genome-wide association study of hematological and biochemical traits in a Japanese population.
Risk Allele G
P-val 3E-7
Odds Ratio .12 [0.076-0.170] unit decrease