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rs2298574

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs2298574(A;G)
Make rs2298574(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position27989094
GeneCDH2
is asnp
is mentioned by
dbSNPrs2298574
ebirs2298574
HLIrs2298574
Exacrs2298574
Varsomers2298574
Maprs2298574
PheGenIrs2298574
hapmaprs2298574
1000 genomesrs2298574
hgdprs2298574
ensemblrs2298574
gopubmedrs2298574
geneviewrs2298574
scholarrs2298574
googlers2298574
pharmgkbrs2298574
gwascentralrs2298574
openSNPrs2298574
23andMers2298574
23andMe allrs2298574
SNP Nexus

SNPshotrs2298574
SNPdbers2298574
MSV3drs2298574
GWAS Ctlgrs2298574
GMAF0.06198
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21810271OA-icon.png]
Trait
Title Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
Risk Allele G
P-val 0.000006
Odds Ratio 0.2700 [0.15-0.39] IU/dL decrease