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rs6918981

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs6918981(A;G)
Make rs6918981(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position34270737
is asnp
is mentioned by
dbSNPrs6918981
ebirs6918981
HLIrs6918981
Exacrs6918981
Varsomers6918981
Maprs6918981
PheGenIrs6918981
hapmaprs6918981
1000 genomesrs6918981
hgdprs6918981
ensemblrs6918981
gopubmedrs6918981
geneviewrs6918981
scholarrs6918981
googlers6918981
pharmgkbrs6918981
gwascentralrs6918981
openSNPrs6918981
23andMers6918981
23andMe allrs6918981
SNP Nexus

SNPshotrs6918981
SNPdbers6918981
MSV3drs6918981
GWAS Ctlgrs6918981
GMAF0.3154
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19396169]
Trait Height
Title A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
Risk Allele G
P-val 3E-8
Odds Ratio 0.40 [0.26-0.54] cm increase
GWAS snp
PMID [PMID 19893584]
Trait Height
Title Identification of 15 loci influencing height in a Korean population
Risk Allele G
P-val 2E-8
Odds Ratio 0.55 [NR] cm increase


GET Evidence
rs6918981
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.664062
summary