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rs2269372

From SNPedia

Orientationplus
Stabilizedplus
Make rs2269372(A;A)
Make rs2269372(A;G)
Make rs2269372(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153942092
GeneRENBP
is asnp
is mentioned by
dbSNPrs2269372
ebirs2269372
HLIrs2269372
Exacrs2269372
Varsomers2269372
Maprs2269372
PheGenIrs2269372
hapmaprs2269372
1000 genomesrs2269372
hgdprs2269372
ensemblrs2269372
gopubmedrs2269372
geneviewrs2269372
scholarrs2269372
googlers2269372
pharmgkbrs2269372
gwascentralrs2269372
openSNPrs2269372
23andMers2269372
23andMe allrs2269372
SNP Nexus

SNPshotrs2269372
SNPdbers2269372
MSV3drs2269372
GWAS Ctlgrs2269372
GMAF0.494
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20486282OA-icon.png] Genetic variants in the renin-angiotensin-aldosterone system and salt sensitivity of blood pressure


[PMID 18520591OA-icon.png] Sequence variants in host cell factor C1 are associated with Meniere's disease.


[PMID 24043878OA-icon.png] Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese