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rs7042864

From SNPedia

Orientationplus
Stabilizedplus
Make rs7042864(C;C)
Make rs7042864(C;T)
Make rs7042864(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position108110027
is asnp
is mentioned by
dbSNPrs7042864
ebirs7042864
HLIrs7042864
Exacrs7042864
Varsomers7042864
Maprs7042864
PheGenIrs7042864
hapmaprs7042864
1000 genomesrs7042864
hgdprs7042864
ensemblrs7042864
gopubmedrs7042864
geneviewrs7042864
scholarrs7042864
googlers7042864
pharmgkbrs7042864
gwascentralrs7042864
openSNPrs7042864
23andMers7042864
23andMe allrs7042864
SNP Nexus

SNPshotrs7042864
SNPdbers7042864
MSV3drs7042864
GWAS Ctlgrs7042864
GMAF0.2649
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903302OA-icon.png]
Trait Tonometry
Title Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
Risk Allele
P-val 0.0000060000000000000002
Odds Ratio NR NR


GET Evidence
rs7042864
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.265625
summary