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rs16969681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16969681(C;T)
Make rs16969681(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position32700910
is asnp
is mentioned by
dbSNPrs16969681
ebirs16969681
HLIrs16969681
Exacrs16969681
Varsomers16969681
Maprs16969681
PheGenIrs16969681
hapmaprs16969681
1000 genomesrs16969681
hgdprs16969681
ensemblrs16969681
gopubmedrs16969681
geneviewrs16969681
scholarrs16969681
googlers16969681
pharmgkbrs16969681
gwascentralrs16969681
openSNPrs16969681
23andMers16969681
23andMe allrs16969681
SNP Nexus

SNPshotrs16969681
SNPdbers16969681
MSV3drs16969681
GWAS Ctlgrs16969681
GMAF0.1768
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 21655089OA-icon.png] Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer


[PMID 26043427] Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population