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rs16985615

From SNPedia

Orientationplus
Stabilizedplus
Make rs16985615(C;C)
Make rs16985615(C;T)
Make rs16985615(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position23661790
is asnp
is mentioned by
dbSNPrs16985615
ebirs16985615
HLIrs16985615
Exacrs16985615
Varsomers16985615
Maprs16985615
PheGenIrs16985615
hapmaprs16985615
1000 genomesrs16985615
hgdprs16985615
ensemblrs16985615
gopubmedrs16985615
geneviewrs16985615
scholarrs16985615
googlers16985615
pharmgkbrs16985615
gwascentralrs16985615
openSNPrs16985615
23andMers16985615
23andMe allrs16985615
SNP Nexus

SNPshotrs16985615
SNPdbers16985615
MSV3drs16985615
GWAS Ctlgrs16985615
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24952865]
Trait Plasma cystastin c levels in acute coronary syndrome
Title Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet inhibition and patient Outcomes study.
Risk Allele
P-val 4E-7
Odds Ratio NR NR