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rs3813800

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs3813800(C;C)
Make rs3813800(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position27370983
GeneFCN3
is asnp
is mentioned by
dbSNPrs3813800
ebirs3813800
HLIrs3813800
Exacrs3813800
Varsomers3813800
Maprs3813800
PheGenIrs3813800
hapmaprs3813800
1000 genomesrs3813800
hgdprs3813800
ensemblrs3813800
gopubmedrs3813800
geneviewrs3813800
scholarrs3813800
googlers3813800
pharmgkbrs3813800
gwascentralrs3813800
openSNPrs3813800
23andMers3813800
23andMe allrs3813800
SNP Nexus

SNPshotrs3813800
SNPdbers3813800
MSV3drs3813800
GWAS Ctlgrs3813800
GMAF0.05601
Max Magnitude0
? (C;C) (C;G) (G;G) 28

[PMID 22471352] A Common Genetic Variant of FCN3/CD164L2 Is Associated with Essential Hypertension in a Chinese Population