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rs7104908

From SNPedia

Orientationplus
Stabilizedplus
Make rs7104908(A;A)
Make rs7104908(A;G)
Make rs7104908(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position76256419
is asnp
is mentioned by
dbSNPrs7104908
ebirs7104908
HLIrs7104908
Exacrs7104908
Varsomers7104908
Maprs7104908
PheGenIrs7104908
hapmaprs7104908
1000 genomesrs7104908
hgdprs7104908
ensemblrs7104908
gopubmedrs7104908
geneviewrs7104908
scholarrs7104908
googlers7104908
pharmgkbrs7104908
gwascentralrs7104908
openSNPrs7104908
23andMers7104908
23andMe allrs7104908
SNP Nexus

SNPshotrs7104908
SNPdbers7104908
MSV3drs7104908
GWAS Ctlgrs7104908
GMAF0.4137
Max Magnitude

[PMID 22679278] Association of polymorphisms in prolylcarboxypeptidase and chymase genes with essential hypertension in the Chinese Han population