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rs7550636

From SNPedia

Orientationplus
Stabilizedplus
Make rs7550636(C;C)
Make rs7550636(C;T)
Make rs7550636(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position192837111
is asnp
is mentioned by
dbSNPrs7550636
ebirs7550636
HLIrs7550636
Exacrs7550636
Varsomers7550636
Maprs7550636
PheGenIrs7550636
hapmaprs7550636
1000 genomesrs7550636
hgdprs7550636
ensemblrs7550636
gopubmedrs7550636
geneviewrs7550636
scholarrs7550636
googlers7550636
pharmgkbrs7550636
gwascentralrs7550636
openSNPrs7550636
23andMers7550636
23andMe allrs7550636
SNP Nexus

SNPshotrs7550636
SNPdbers7550636
MSV3drs7550636
GWAS Ctlgrs7550636
GMAF0.2934
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23870195OA-icon.png]
Trait Coronary artery calcification
Title Genetics of coronary artery calcification among African Americans, a meta-analysis.
Risk Allele T
P-val 4E-6
Odds Ratio .25 [0.13-0.37] unit decrease