Have questions? Visit https://www.reddit.com/r/SNPedia

rs4758685

From SNPedia

Orientationminus
Stabilizedminus
Make rs4758685(C;C)
Make rs4758685(C;T)
Make rs4758685(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position122142295
GeneMLXIP
is asnp
is mentioned by
dbSNPrs4758685
ClinGenrs4758685
ebirs4758685
HLIrs4758685
Exacrs4758685
Varsomers4758685
Maprs4758685
PheGenIrs4758685
hapmaprs4758685
1000 genomesrs4758685
hgdprs4758685
ensemblrs4758685
gopubmedrs4758685
geneviewrs4758685
scholarrs4758685
googlers4758685
pharmgkbrs4758685
gwascentralrs4758685
openSNPrs4758685
23andMers4758685
23andMe allrs4758685
SNP Nexus

SNPshotrs4758685
SNPdbers4758685
MSV3drs4758685
GWAS Ctlgrs4758685
GMAF0.4936
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23840567OA-icon.png] The Association Study between Twenty One Polymorphisms in Seven Candidate Genes and Coronary Heart Diseases in Chinese Han Population