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rs4789932

From SNPedia

Orientationminus
Stabilizedminus
Make rs4789932(C;C)
Make rs4789932(C;T)
Make rs4789932(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position78928193
is asnp
is mentioned by
dbSNPrs4789932
ebirs4789932
HLIrs4789932
Exacrs4789932
Varsomers4789932
Maprs4789932
PheGenIrs4789932
hapmaprs4789932
1000 genomesrs4789932
hgdprs4789932
ensemblrs4789932
gopubmedrs4789932
geneviewrs4789932
scholarrs4789932
googlers4789932
pharmgkbrs4789932
gwascentralrs4789932
openSNPrs4789932
23andMers4789932
23andMe allrs4789932
SNP Nexus

SNPshotrs4789932
SNPdbers4789932
MSV3drs4789932
GWAS Ctlgrs4789932
GMAF0.4711
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23491141] Polymorphic variation within the ADAMTS2, ADAMTS14, ADAMTS5, ADAM12 and TIMP2 genes and the risk of Achilles tendon pathology: A genetic association study


[PMID 19431211OA-icon.png] Polymorphisms in tissue inhibitors of metalloproteinases-2 and -3 and breast cancer susceptibility and survival.