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rs1400544

From SNPedia

Orientationminus
Stabilizedminus
Make rs1400544(A;A)
Make rs1400544(A;T)
Make rs1400544(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position189892274
is asnp
is mentioned by
dbSNPrs1400544
ebirs1400544
HLIrs1400544
Exacrs1400544
Varsomers1400544
Maprs1400544
PheGenIrs1400544
hapmaprs1400544
1000 genomesrs1400544
hgdprs1400544
ensemblrs1400544
gopubmedrs1400544
geneviewrs1400544
scholarrs1400544
googlers1400544
pharmgkbrs1400544
gwascentralrs1400544
openSNPrs1400544
23andMers1400544
23andMe allrs1400544
SNP Nexus

SNPshotrs1400544
SNPdbers1400544
MSV3drs1400544
GWAS Ctlgrs1400544
GMAF0.2746
Max Magnitude
? (A;A) (A;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
rs1400544
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.325397
summary