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rs6733301

From SNPedia

Orientationplus
Stabilizedplus
Make rs6733301(A;A)
Make rs6733301(A;G)
Make rs6733301(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position25053415
GeneEFR3B
is asnp
is mentioned by
dbSNPrs6733301
ebirs6733301
HLIrs6733301
Exacrs6733301
Varsomers6733301
Maprs6733301
PheGenIrs6733301
hapmaprs6733301
1000 genomesrs6733301
hgdprs6733301
ensemblrs6733301
gopubmedrs6733301
geneviewrs6733301
scholarrs6733301
googlers6733301
pharmgkbrs6733301
gwascentralrs6733301
openSNPrs6733301
23andMers6733301
23andMe allrs6733301
SNP Nexus

SNPshotrs6733301
SNPdbers6733301
MSV3drs6733301
GWAS Ctlgrs6733301
GMAF0.0877
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 7.9999999999999996E-7
Odds Ratio 7.50 [4.56-10.44] % SD taller


GET Evidence
rs6733301
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary