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rs587777929

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777929(C;T)
Make rs587777929(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position73252803
GeneCCT7
is asnp
is mentioned by
dbSNPrs587777929
ebirs587777929
HLIrs587777929
Exacrs587777929
Varsomers587777929
Maprs587777929
PheGenIrs587777929
hapmaprs587777929
1000 genomesrs587777929
hgdprs587777929
ensemblrs587777929
gopubmedrs587777929
geneviewrs587777929
scholarrs587777929
googlers587777929
pharmgkbrs587777929
gwascentralrs587777929
openSNPrs587777929
23andMers587777929
23andMe allrs587777929
SNP Nexus

SNPshotrs587777929
SNPdbers587777929
MSV3drs587777929
GWAS Ctlgrs587777929
Max Magnitude0
ClinVar
Risk rs587777929(T;T)
Alt rs587777929(T;T)
Reference rs587777929(C;C)
Significance Pathogenic
Disease Myocardial infarction 1
Variation info
Gene CCT7
CLNDBN Myocardial infarction 1
Reversed 0
HGVS NC_000002.11:g.73479931C>T
CLNSRC
CLNACC RCV000077778.1,