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rs1367248

From SNPedia

Orientationplus
Stabilizedplus
Make rs1367248(G;G)
Make rs1367248(G;T)
Make rs1367248(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position124240787
GeneCNTNAP5
is asnp
is mentioned by
dbSNPrs1367248
ebirs1367248
HLIrs1367248
Exacrs1367248
Varsomers1367248
Maprs1367248
PheGenIrs1367248
hapmaprs1367248
1000 genomesrs1367248
hgdprs1367248
ensemblrs1367248
gopubmedrs1367248
geneviewrs1367248
scholarrs1367248
googlers1367248
pharmgkbrs1367248
gwascentralrs1367248
openSNPrs1367248
23andMers1367248
23andMe allrs1367248
SNP Nexus

SNPshotrs1367248
SNPdbers1367248
MSV3drs1367248
GWAS Ctlgrs1367248
GMAF0.1961
Max Magnitude
? (G;G) (G;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 0.0000030000000000000001
Odds Ratio NR NR


GET Evidence
rs1367248
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary