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rs4713858

From SNPedia

Orientationplus
Stabilizedplus
Make rs4713858(A;A)
Make rs4713858(A;G)
Make rs4713858(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position35435008
is asnp
is mentioned by
dbSNPrs4713858
ebirs4713858
HLIrs4713858
Exacrs4713858
Varsomers4713858
Maprs4713858
PheGenIrs4713858
hapmaprs4713858
1000 genomesrs4713858
hgdprs4713858
ensemblrs4713858
gopubmedrs4713858
geneviewrs4713858
scholarrs4713858
googlers4713858
pharmgkbrs4713858
gwascentralrs4713858
openSNPrs4713858
23andMers4713858
23andMe allrs4713858
SNP Nexus

SNPshotrs4713858
SNPdbers4713858
MSV3drs4713858
GWAS Ctlgrs4713858
GMAF0.152
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele G
P-val 4E-8
Odds Ratio 6.80 [4.45-9.15] % SD taller


[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


[PMID 19039035OA-icon.png] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.


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


GET Evidence
rs4713858
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.84375
summary