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rs2638953

From SNPedia

Orientationminus
Stabilizedminus
Make rs2638953(C;C)
Make rs2638953(C;G)
Make rs2638953(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position28381482
GeneCCDC91
is asnp
is mentioned by
dbSNPrs2638953
ebirs2638953
HLIrs2638953
Exacrs2638953
Varsomers2638953
Maprs2638953
PheGenIrs2638953
hapmaprs2638953
1000 genomesrs2638953
hgdprs2638953
ensemblrs2638953
gopubmedrs2638953
geneviewrs2638953
scholarrs2638953
googlers2638953
pharmgkbrs2638953
gwascentralrs2638953
openSNPrs2638953
23andMers2638953
23andMe allrs2638953
SNP Nexus

SNPshotrs2638953
SNPdbers2638953
MSV3drs2638953
GWAS Ctlgrs2638953
GMAF0.2456
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height
Risk Allele C
P-val 7E-17
Odds Ratio 0.03 [NR] unit increase