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rs12651106

From SNPedia

Orientationplus
Stabilizedplus
Make rs12651106(A;A)
Make rs12651106(A;C)
Make rs12651106(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position154379907
GeneDCHS2
is asnp
is mentioned by
dbSNPrs12651106
ebirs12651106
HLIrs12651106
Exacrs12651106
Varsomers12651106
Maprs12651106
PheGenIrs12651106
hapmaprs12651106
1000 genomesrs12651106
hgdprs12651106
ensemblrs12651106
gopubmedrs12651106
geneviewrs12651106
scholarrs12651106
googlers12651106
pharmgkbrs12651106
gwascentralrs12651106
openSNPrs12651106
23andMers12651106
23andMe allrs12651106
SNP Nexus

SNPshotrs12651106
SNPdbers12651106
MSV3drs12651106
GWAS Ctlgrs12651106
GMAF0.1382
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21757653OA-icon.png]
Trait
Title Association of {gamma}' Fibrinogen With Cardiovascular Disease.
Risk Allele A
P-val 2E-12
Odds Ratio 0.1400 [0.10-0.18] g/L decrease