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rs516246

From SNPedia

Orientationminus
Stabilizedminus
Make rs516246(A;A)
Make rs516246(A;G)
Make rs516246(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position48702915
GeneFUT2, LOC105447645
is asnp
is mentioned by
dbSNPrs516246
dbSNP (classic)rs516246
ClinGenrs516246
ebirs516246
HLIrs516246
Exacrs516246
Gnomadrs516246
Varsomers516246
LitVarrs516246
Maprs516246
PheGenIrs516246
Biobankrs516246
1000 genomesrs516246
hgdprs516246
ensemblrs516246
geneviewrs516246
scholarrs516246
googlers516246
pharmgkbrs516246
gwascentralrs516246
openSNPrs516246
23andMers516246
SNPshotrs516246
SNPdbers516246
MSV3drs516246
GWAS Ctlgrs516246
GMAF0.3242
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22001757OA-icon.png]
Trait
Title Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
Risk Allele T
P-val 8E-10
Odds Ratio 2.3000 None
GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Crohn's disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele T
P-val 1E-15
Odds Ratio 1.11 [1.071-1.143]
GWAS snp
PMID [PMID 23251661OA-icon.png]
Trait Obesity-related traits
Title Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele A
P-val 2E-6
Odds Ratio .03 [NR] pmol/L increase