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rs10486715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10486715(A;A)
Make rs10486715(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position41439010
is asnp
is mentioned by
dbSNPrs10486715
ebirs10486715
HLIrs10486715
Exacrs10486715
Varsomers10486715
Maprs10486715
PheGenIrs10486715
hapmaprs10486715
1000 genomesrs10486715
hgdprs10486715
ensemblrs10486715
gopubmedrs10486715
geneviewrs10486715
scholarrs10486715
googlers10486715
pharmgkbrs10486715
gwascentralrs10486715
openSNPrs10486715
23andMers10486715
23andMe allrs10486715
SNP Nexus

SNPshotrs10486715
SNPdbers10486715
MSV3drs10486715
GWAS Ctlgrs10486715
GMAF0.1763
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele A
P-val 0.000003
Odds Ratio 0.44 [NR] inch decrease

height being the quantitative trait associated with in [PMID 19197348OA-icon.png]


GET Evidence
rs10486715
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary