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rs10794501

From SNPedia

Orientationplus
Stabilizedplus
Make rs10794501(A;A)
Make rs10794501(A;T)
Make rs10794501(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position27372958
GeneFCN3
is asnp
is mentioned by
dbSNPrs10794501
ebirs10794501
HLIrs10794501
Exacrs10794501
Varsomers10794501
Maprs10794501
PheGenIrs10794501
hapmaprs10794501
1000 genomesrs10794501
hgdprs10794501
ensemblrs10794501
gopubmedrs10794501
geneviewrs10794501
scholarrs10794501
googlers10794501
pharmgkbrs10794501
gwascentralrs10794501
openSNPrs10794501
23andMers10794501
23andMe allrs10794501
SNP Nexus

SNPshotrs10794501
SNPdbers10794501
MSV3drs10794501
GWAS Ctlgrs10794501
GMAF0.2769
Max Magnitude
? (A;A) (A;T) (T;T) 28

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

[PMID 19220833OA-icon.png] Exploring the role of polymorphisms in ficolin genes in respiratory tract infections in children.