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rs7069923

From SNPedia

Orientationplus
Stabilizedplus
Make rs7069923(C;C)
Make rs7069923(C;T)
Make rs7069923(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position18441439
GeneCACNB2
is asnp
is mentioned by
dbSNPrs7069923
ebirs7069923
HLIrs7069923
Exacrs7069923
Varsomers7069923
Maprs7069923
PheGenIrs7069923
hapmaprs7069923
1000 genomesrs7069923
hgdprs7069923
ensemblrs7069923
gopubmedrs7069923
geneviewrs7069923
scholarrs7069923
googlers7069923
pharmgkbrs7069923
gwascentralrs7069923
openSNPrs7069923
23andMers7069923
23andMe allrs7069923
SNP Nexus

SNPshotrs7069923
SNPdbers7069923
MSV3drs7069923
GWAS Ctlgrs7069923
GMAF0.4013
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele C
P-val 0.000001
Odds Ratio 0.19 [NR] mm Hg increase

systolic blood pressure being the quantitative trait associated with in [PMID 19197348OA-icon.png]


GET Evidence
rs7069923
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.359375
summary