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rs2235306

From SNPedia

Orientationplus
Stabilizedplus
Make rs2235306(C;C)
Make rs2235306(C;T)
Make rs2235306(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position129650121
GeneAPLN
is asnp
is mentioned by
dbSNPrs2235306
ebirs2235306
HLIrs2235306
Exacrs2235306
Varsomers2235306
Maprs2235306
PheGenIrs2235306
hapmaprs2235306
1000 genomesrs2235306
hgdprs2235306
ensemblrs2235306
gopubmedrs2235306
geneviewrs2235306
scholarrs2235306
googlers2235306
pharmgkbrs2235306
gwascentralrs2235306
openSNPrs2235306
23andMers2235306
23andMe allrs2235306
SNP Nexus

SNPshotrs2235306
SNPdbers2235306
MSV3drs2235306
GWAS Ctlgrs2235306
GMAF0.234
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20224560OA-icon.png] Association of genetic variants in the apelin-APJ system and ACE2 with blood pressure responses to potassium supplementation: the GenSalt study.

[PMID 19567136] Association of apelin genetic variants with type 2 diabetes and related clinical features in Chinese Hans.

[PMID 20125035OA-icon.png] Genetic variants in the apelin system and blood pressure responses to dietary sodium interventions: a family-based association study.