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rs2504778

From SNPedia

Orientationplus
Stabilizedplus
Make rs2504778(A;A)
Make rs2504778(A;G)
Make rs2504778(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position27381490
GeneCD164L2
is asnp
is mentioned by
dbSNPrs2504778
ebirs2504778
HLIrs2504778
Exacrs2504778
Varsomers2504778
Maprs2504778
PheGenIrs2504778
hapmaprs2504778
1000 genomesrs2504778
hgdprs2504778
ensemblrs2504778
gopubmedrs2504778
geneviewrs2504778
scholarrs2504778
googlers2504778
pharmgkbrs2504778
gwascentralrs2504778
openSNPrs2504778
23andMers2504778
23andMe allrs2504778
SNP Nexus

SNPshotrs2504778
SNPdbers2504778
MSV3drs2504778
GWAS Ctlgrs2504778
GMAF0.2792
Max Magnitude
? (A;A) (A;G) (G;G) 28

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