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rs274557

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs274557(A;G)
Make rs274557(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position132385512
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs274557
dbSNP (classic)rs274557
ClinGenrs274557
ebirs274557
HLIrs274557
Exacrs274557
Gnomadrs274557
Varsomers274557
LitVarrs274557
Maprs274557
PheGenIrs274557
Biobankrs274557
1000 genomesrs274557
hgdprs274557
ensemblrs274557
geneviewrs274557
scholarrs274557
googlers274557
pharmgkbrs274557
gwascentralrs274557
openSNPrs274557
23andMers274557
SNPshotrs274557
SNPdbers274557
MSV3drs274557
GWAS Ctlgrs274557
Max Magnitude0
GWAS snp
PMID [PMID 24823311OA-icon.png]
Trait Plasma omega-6 polyunsaturated fatty acid levels (arachidonic acid)
Title Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium.
Risk Allele T
P-val 4E-6
Odds Ratio .14 [NR] unit increase


ClinVar
Risk rs274557(G;G)
Alt rs274557(G;G)
Reference Rs274557(A;A)
Significance Non-pathogenic
Disease Renal carnitine transport defect not specified
Variation info
Gene SLC22A5
CLNDBN Renal carnitine transport defect not specified
Reversed 1
HGVS NC_000005.9:g.131721204T\x3d; NC_000005.9:g.131721204T>C
CLNSRC ClinVar
CLNACC RCV000022347.2, RCV000080061.5, RCV000303629.1,