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rs1151640

From SNPedia

Orientationminus
Stabilizedminus
Make rs1151640(A;A)
Make rs1151640(A;G)
Make rs1151640(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position247672648
GeneOR13G1
is asnp
is mentioned by
dbSNPrs1151640
ebirs1151640
HLIrs1151640
Exacrs1151640
Varsomers1151640
Maprs1151640
PheGenIrs1151640
hapmaprs1151640
1000 genomesrs1151640
hgdprs1151640
ensemblrs1151640
gopubmedrs1151640
geneviewrs1151640
scholarrs1151640
googlers1151640
pharmgkbrs1151640
gwascentralrs1151640
openSNPrs1151640
23andMers1151640
23andMe allrs1151640
SNP Nexus

SNPshotrs1151640
SNPdbers1151640
MSV3drs1151640
GWAS Ctlgrs1151640
GMAF0.4394
Max Magnitude
? (A;A) (A;G) (G;G) 28
rs1151640 increases susceptibility to Myocardial Infarction 1.31 times for heterozygotes (AG) and 1.40 times for homozygotes (GG) [PMID 16175505OA-icon.png]

An independent study of 3657 patients with myocardial infarction (885 women and 2772 men) and 1211 control individuals (598 women and 613 men) did not observe any correlation to this SNP.[PMID 19709766]


[PMID 18599554OA-icon.png] Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia.


[PMID 20017983OA-icon.png] Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.


GET Evidence
OR13G1-I132V
aa_change Ile132Val
aa_change_short I132V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.335285
summary