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rs7249094

From SNPedia

Orientationplus
Stabilizedplus
Make rs7249094(A;A)
Make rs7249094(A;G)
Make rs7249094(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position8607115
GeneADAMTS10
is asnp
is mentioned by
dbSNPrs7249094
ebirs7249094
HLIrs7249094
Exacrs7249094
Varsomers7249094
Maprs7249094
PheGenIrs7249094
hapmaprs7249094
1000 genomesrs7249094
hgdprs7249094
ensemblrs7249094
gopubmedrs7249094
geneviewrs7249094
scholarrs7249094
googlers7249094
pharmgkbrs7249094
gwascentralrs7249094
openSNPrs7249094
23andMers7249094
23andMe allrs7249094
SNP Nexus

SNPshotrs7249094
SNPdbers7249094
MSV3drs7249094
GWAS Ctlgrs7249094
GMAF0.4353
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 9.9999999999999995E-7
Odds Ratio 4.30 [2.54-6.06] % SD taller


GET Evidence
rs7249094
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.515625
summary