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rs678962

From SNPedia

Orientationplus
Stabilizedplus
Make rs678962(G;G)
Make rs678962(G;T)
Make rs678962(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position172220749
GeneDNM3
is asnp
is mentioned by
dbSNPrs678962
ebirs678962
HLIrs678962
Exacrs678962
Varsomers678962
Maprs678962
PheGenIrs678962
hapmaprs678962
1000 genomesrs678962
hgdprs678962
ensemblrs678962
gopubmedrs678962
geneviewrs678962
scholarrs678962
googlers678962
pharmgkbrs678962
gwascentralrs678962
openSNPrs678962
23andMers678962
23andMe allrs678962
SNP Nexus

SNPshotrs678962
SNPdbers678962
MSV3drs678962
GWAS Ctlgrs678962
GMAF0.2645
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele G
P-val 2.9999999999999997E-8
Odds Ratio 5.40 [3.44-7.36] % SD taller


[PMID 19197348OA-icon.png] Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.


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


GET Evidence
rs678962
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary