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rs2675609

From SNPedia

Orientationplus
Stabilizedplus
Make rs2675609(C;C)
Make rs2675609(C;T)
Make rs2675609(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position61876772
is asnp
is mentioned by
dbSNPrs2675609
dbSNP (classic)rs2675609
ClinGenrs2675609
ebirs2675609
HLIrs2675609
Exacrs2675609
Gnomadrs2675609
Varsomers2675609
LitVarrs2675609
Maprs2675609
PheGenIrs2675609
Biobankrs2675609
1000 genomesrs2675609
hgdprs2675609
ensemblrs2675609
geneviewrs2675609
scholarrs2675609
googlers2675609
pharmgkbrs2675609
gwascentralrs2675609
openSNPrs2675609
23andMers2675609
SNPshotrs2675609
SNPdbers2675609
MSV3drs2675609
GWAS Ctlgrs2675609
GMAF0.4311
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23022100OA-icon.png]
Trait Serum total protein level
Title Discovery and fine mapping of serum protein loci through transethnic meta-analysis.
Risk Allele T
P-val 2E-6
Odds Ratio .04 [0.022-0.050] unit decrease