Have questions? Visit https://www.reddit.com/r/SNPedia

rs3760318

From SNPedia

Orientationminus
Stabilizedminus
Make rs3760318(C;C)
Make rs3760318(C;T)
Make rs3760318(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position30920697
GeneADAP2
is asnp
is mentioned by
dbSNPrs3760318
ebirs3760318
HLIrs3760318
Exacrs3760318
Varsomers3760318
Maprs3760318
PheGenIrs3760318
hapmaprs3760318
1000 genomesrs3760318
hgdprs3760318
ensemblrs3760318
gopubmedrs3760318
geneviewrs3760318
scholarrs3760318
googlers3760318
pharmgkbrs3760318
gwascentralrs3760318
openSNPrs3760318
23andMers3760318
23andMe allrs3760318
SNP Nexus

SNPshotrs3760318
SNPdbers3760318
MSV3drs3760318
GWAS Ctlgrs3760318
GMAF0.3558
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele C
P-val 2.0000000000000001E-9
Odds Ratio 6.00 [4.04-7.96] % SD taller  % SD taller


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


[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
rs3760318
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.414062
summary