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rs6495122

From SNPedia

Orientationplus
Stabilizedplus
Make rs6495122(A;A)
Make rs6495122(A;C)
Make rs6495122(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position74833304
GeneCPLX3
is asnp
is mentioned by
dbSNPrs6495122
ebirs6495122
HLIrs6495122
Exacrs6495122
Varsomers6495122
Maprs6495122
PheGenIrs6495122
hapmaprs6495122
1000 genomesrs6495122
hgdprs6495122
ensemblrs6495122
gopubmedrs6495122
geneviewrs6495122
scholarrs6495122
googlers6495122
pharmgkbrs6495122
gwascentralrs6495122
openSNPrs6495122
23andMers6495122
23andMe allrs6495122
SNP Nexus

SNPshotrs6495122
SNPdbers6495122
MSV3drs6495122
GWAS Ctlgrs6495122
GMAF0.3522
Max Magnitude
? (A;A) (A;C) (C;C) 28
23andMe blog blood pressure
GWAS snp
PMID [PMID 19430479OA-icon.png]
Trait Diastolic Blood Pressure
Title Genome-wide association study of blood pressure and hypertension
Risk Allele A
P-val 2E-10
Odds Ratio 0.40 [0.28-0.52] mm Hg increase
GWAS snp
PMID [PMID 21490707OA-icon.png]
Trait
Title Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.
Risk Allele A
P-val 6E-7
Odds Ratio 0.0700 [0.05-0.09] mg/day decrease
GWAS snp
PMID [PMID 21876539OA-icon.png]
Trait
Title Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM.
Risk Allele A
P-val 7E-9
Odds Ratio 0.0500 [0.03-0.07] unit decrease


GET Evidence
rs6495122
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.288136
summary