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rs6692700

From SNPedia

Orientationplus
Stabilizedplus
Make rs6692700(A;A)
Make rs6692700(A;C)
Make rs6692700(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position238506476
is asnp
is mentioned by
dbSNPrs6692700
ebirs6692700
HLIrs6692700
Exacrs6692700
Varsomers6692700
Maprs6692700
PheGenIrs6692700
hapmaprs6692700
1000 genomesrs6692700
hgdprs6692700
ensemblrs6692700
gopubmedrs6692700
geneviewrs6692700
scholarrs6692700
googlers6692700
pharmgkbrs6692700
gwascentralrs6692700
openSNPrs6692700
23andMers6692700
23andMe allrs6692700
SNP Nexus

SNPshotrs6692700
SNPdbers6692700
MSV3drs6692700
GWAS Ctlgrs6692700
GMAF0.4706
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23698163OA-icon.png]
Trait Serum selenium levels
Title Genome-wide association study of serum selenium concentrations.
Risk Allele
P-val 2E-6
Odds Ratio .04 [0.024-0.056] mg/dL increase