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rs1320267

From SNPedia

Orientationplus
Stabilizedplus
Make rs1320267(C;C)
Make rs1320267(C;G)
Make rs1320267(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position126012137
is asnp
is mentioned by
dbSNPrs1320267
ebirs1320267
HLIrs1320267
Exacrs1320267
Varsomers1320267
Maprs1320267
PheGenIrs1320267
hapmaprs1320267
1000 genomesrs1320267
hgdprs1320267
ensemblrs1320267
gopubmedrs1320267
geneviewrs1320267
scholarrs1320267
googlers1320267
pharmgkbrs1320267
gwascentralrs1320267
openSNPrs1320267
23andMers1320267
23andMe allrs1320267
SNP Nexus

SNPshotrs1320267
SNPdbers1320267
MSV3drs1320267
GWAS Ctlgrs1320267
GMAF0.4183
Max Magnitude
? (C;C) (C;G) (G;G) 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 0.0000069999999999999999
Odds Ratio NR NR


GET Evidence
rs1320267
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.403226
summary