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rs2889529

From SNPedia

Orientationminus
Stabilizedminus
Make rs2889529(C;C)
Make rs2889529(C;T)
Make rs2889529(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position78901393
GeneLOC100653515, TIMP2
is asnp
is mentioned by
dbSNPrs2889529
ebirs2889529
HLIrs2889529
Exacrs2889529
Varsomers2889529
Maprs2889529
PheGenIrs2889529
hapmaprs2889529
1000 genomesrs2889529
hgdprs2889529
ensemblrs2889529
gopubmedrs2889529
geneviewrs2889529
scholarrs2889529
googlers2889529
pharmgkbrs2889529
gwascentralrs2889529
openSNPrs2889529
23andMers2889529
23andMe allrs2889529
SNP Nexus

SNPshotrs2889529
SNPdbers2889529
MSV3drs2889529
GWAS Ctlgrs2889529
GMAF0.4573
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM277470
DescPONTOCEREBELLAR HYPOPLASIA TYPE 2A; PCH2A
Variant
Relatedalso
[PMID 17903307OA-icon.png] Framingham Heart Study genome-wide association: results for pulmonary function measures.