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

rs1109748

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1109748(A;A)
Make rs1109748(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position61955173
GeneBEST1
is asnp
is mentioned by
dbSNPrs1109748
ebirs1109748
HLIrs1109748
Exacrs1109748
Varsomers1109748
Maprs1109748
PheGenIrs1109748
hapmaprs1109748
1000 genomesrs1109748
hgdprs1109748
ensemblrs1109748
gopubmedrs1109748
geneviewrs1109748
scholarrs1109748
googlers1109748
pharmgkbrs1109748
gwascentralrs1109748
openSNPrs1109748
23andMers1109748
23andMe allrs1109748
SNP Nexus

SNPshotrs1109748
SNPdbers1109748
MSV3drs1109748
GWAS Ctlgrs1109748
GMAF0.2741
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21829377OA-icon.png]
Trait
Title Genetic Loci Associated with Plasma Phospholipid n-3 Fatty Acids: A Meta-Analysis of Genome-Wide Association Studies from the CHARGE Consortium.
Risk Allele A
P-val 5E-9
Odds Ratio 0.0500 [NR] % decrease


ClinVar
Risk rs1109748(A;A)
Alt rs1109748(A;A)
Reference rs1109748(C;C)
Significance Non-pathogenic
Disease not provided not specified
Variation info
Gene BEST1
CLNDBN not provided not specified
Reversed 0
HGVS NC_000011.9:g.61722645C>A
CLNSRC ClinVar Retina International
CLNACC RCV000086102.1, RCV000152862.3,