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rs7871764

From SNPedia

Orientationplus
Stabilizedplus
Make rs7871764(G;G)
Make rs7871764(G;T)
Make rs7871764(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34071543
is asnp
is mentioned by
dbSNPrs7871764
ebirs7871764
HLIrs7871764
Exacrs7871764
Varsomers7871764
Maprs7871764
PheGenIrs7871764
hapmaprs7871764
1000 genomesrs7871764
hgdprs7871764
ensemblrs7871764
gopubmedrs7871764
geneviewrs7871764
scholarrs7871764
googlers7871764
pharmgkbrs7871764
gwascentralrs7871764
openSNPrs7871764
23andMers7871764
23andMe allrs7871764
SNP Nexus

SNPshotrs7871764
SNPdbers7871764
MSV3drs7871764
GWAS Ctlgrs7871764
GMAF0.3145
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19343178OA-icon.png]
Trait Height
Title Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size
Risk Allele
P-val 0.000002
Odds Ratio



GET Evidence
rs7871764
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.65625
summary