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rs10472828

From SNPedia

Orientationplus
Stabilizedplus
Make rs10472828(C;C)
Make rs10472828(C;T)
Make rs10472828(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position32888712
is asnp
is mentioned by
dbSNPrs10472828
dbSNP (old)rs10472828
ClinGenrs10472828
ebirs10472828
HLIrs10472828
Exacrs10472828
Gnomadrs10472828
Varsomers10472828
Maprs10472828
PheGenIrs10472828
Biobankrs10472828
1000 genomesrs10472828
hgdprs10472828
ensemblrs10472828
gopubmedrs10472828
geneviewrs10472828
scholarrs10472828
googlers10472828
pharmgkbrs10472828
gwascentralrs10472828
openSNPrs10472828
23andMers10472828
23andMe allrs10472828
SNP Nexus

SNPshotrs10472828
SNPdbers10472828
MSV3drs10472828
GWAS Ctlgrs10472828
GMAF0.4178
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19343178OA-icon.png]
Trait Height
Title Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size
Risk Allele
P-val 3E-7
Odds Ratio


[PMID 19570815OA-icon.png] A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation


OMIM606255
Desc
Variant
Relatedalso
[PMID 20546612OA-icon.png] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.


GET Evidence
rs10472828
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.335938
summary