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rs16948048

From SNPedia

Orientationplus
Stabilizedplus
Make rs16948048(A;A)
Make rs16948048(A;G)
Make rs16948048(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position49363104
GeneLOC102724596, RP11-1079K10.3, ZNF652
is asnp
is mentioned by
dbSNPrs16948048
ebirs16948048
HLIrs16948048
Exacrs16948048
Varsomers16948048
Maprs16948048
PheGenIrs16948048
hapmaprs16948048
1000 genomesrs16948048
hgdprs16948048
ensemblrs16948048
gopubmedrs16948048
geneviewrs16948048
scholarrs16948048
googlers16948048
pharmgkbrs16948048
gwascentralrs16948048
openSNPrs16948048
23andMers16948048
23andMe allrs16948048
SNP Nexus

SNPshotrs16948048
SNPdbers16948048
MSV3drs16948048
GWAS Ctlgrs16948048
GMAF0.3113
Max Magnitude
? (A;A) (A;G) (G;G) 28
23andMe blog blood pressure
GWAS snp
PMID [PMID 19430483OA-icon.png]
Trait Diastolic Blood Pressure
Title Genome-wide association study identifies eight loci associated with blood pressure
Risk Allele G
P-val 5E-9
Odds Ratio 0.31 [0.21-0.41] mm Hg increase

[PMID 20542020] Confirmation of top polymorphisms in hypertension genome wide association study among Han Chinese.

[PMID 22525200] Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.


GET Evidence
rs16948048
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.320312
summary