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

rs4846085

From SNPedia

Orientationplus
Stabilizedplus
Make rs4846085(C;C)
Make rs4846085(C;T)
Make rs4846085(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position11990577
GeneMFN2
is asnp
is mentioned by
dbSNPrs4846085
ebirs4846085
HLIrs4846085
Exacrs4846085
Varsomers4846085
Maprs4846085
PheGenIrs4846085
hapmaprs4846085
1000 genomesrs4846085
hgdprs4846085
ensemblrs4846085
gopubmedrs4846085
geneviewrs4846085
scholarrs4846085
googlers4846085
pharmgkbrs4846085
gwascentralrs4846085
openSNPrs4846085
23andMers4846085
23andMe allrs4846085
SNP Nexus

SNPshotrs4846085
SNPdbers4846085
MSV3drs4846085
GWAS Ctlgrs4846085
GMAF0.3659
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20940517] HSG/Mfn2 gene polymorphism and essential hypertension: a case-control association study in Chinese