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rs10898392

From SNPedia

Orientationplus
Stabilizedplus
Make rs10898392(G;G)
Make rs10898392(G;T)
Make rs10898392(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position85453707
GeneDLG2
is asnp
is mentioned by
dbSNPrs10898392
ebirs10898392
HLIrs10898392
Exacrs10898392
Varsomers10898392
Maprs10898392
PheGenIrs10898392
hapmaprs10898392
1000 genomesrs10898392
hgdprs10898392
ensemblrs10898392
gopubmedrs10898392
geneviewrs10898392
scholarrs10898392
googlers10898392
pharmgkbrs10898392
gwascentralrs10898392
openSNPrs10898392
23andMers10898392
23andMe allrs10898392
SNP Nexus

SNPshotrs10898392
SNPdbers10898392
MSV3drs10898392
GWAS Ctlgrs10898392
GMAF0.4362
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19570815OA-icon.png]
Trait Height
Title A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
Risk Allele T
P-val 0.000003
Odds Ratio NR NR


GET Evidence
rs10898392
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.380952
summary