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rs2028898

From SNPedia

Orientationminus
Stabilizedplus
Make rs2028898(C;C)
Make rs2028898(C;T)
Make rs2028898(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position85550147
GeneGGCX
is asnp
is mentioned by
dbSNPrs2028898
ebirs2028898
HLIrs2028898
Exacrs2028898
Varsomers2028898
Maprs2028898
PheGenIrs2028898
hapmaprs2028898
1000 genomesrs2028898
hgdprs2028898
ensemblrs2028898
gopubmedrs2028898
geneviewrs2028898
scholarrs2028898
googlers2028898
pharmgkbrs2028898
gwascentralrs2028898
openSNPrs2028898
23andMers2028898
23andMe allrs2028898
SNP Nexus

SNPshotrs2028898
SNPdbers2028898
MSV3drs2028898
GWAS Ctlgrs2028898
GMAF0.3251
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22366784] Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese

[PMID 18535201OA-icon.png] A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.

[PMID 19436136OA-icon.png] Association of sequence variations in vitamin K epoxide reductase and gamma-glutamyl carboxylase genes with biochemical measures of vitamin K status.