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rs7715811

From SNPedia

Orientationplus
Stabilizedplus
Make rs7715811(C;C)
Make rs7715811(C;T)
Make rs7715811(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position13769865
GeneDNAH5
is asnp
is mentioned by
dbSNPrs7715811
ebirs7715811
HLIrs7715811
Exacrs7715811
Varsomers7715811
Maprs7715811
PheGenIrs7715811
hapmaprs7715811
1000 genomesrs7715811
hgdprs7715811
ensemblrs7715811
gopubmedrs7715811
geneviewrs7715811
scholarrs7715811
googlers7715811
pharmgkbrs7715811
gwascentralrs7715811
openSNPrs7715811
23andMers7715811
23andMe allrs7715811
SNP Nexus

SNPshotrs7715811
SNPdbers7715811
MSV3drs7715811
GWAS Ctlgrs7715811
GMAF0.2778
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903303OA-icon.png]
Trait Other subclinical atherosclerosis traits
Title Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study
Risk Allele
P-val 0.0000060000000000000002
Odds Ratio NR NR


GET Evidence
rs7715811
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.335938
summary