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rs13390641

From SNPedia

Orientationplus
Stabilizedplus
Make rs13390641(A;A)
Make rs13390641(A;G)
Make rs13390641(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position103419975
is asnp
is mentioned by
dbSNPrs13390641
ebirs13390641
HLIrs13390641
Exacrs13390641
Varsomers13390641
Maprs13390641
PheGenIrs13390641
hapmaprs13390641
1000 genomesrs13390641
hgdprs13390641
ensemblrs13390641
gopubmedrs13390641
geneviewrs13390641
scholarrs13390641
googlers13390641
pharmgkbrs13390641
gwascentralrs13390641
openSNPrs13390641
23andMers13390641
23andMe allrs13390641
SNP Nexus

SNPshotrs13390641
SNPdbers13390641
MSV3drs13390641
GWAS Ctlgrs13390641
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 24903457OA-icon.png] Identification of a genetic variant at 2q12.1 associated with blood pressure in East-Asians by genome-wide scan including gene-environment interactions