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rs7815788

From SNPedia

Orientationplus
Stabilizedplus
Make rs7815788(C;C)
Make rs7815788(C;T)
Make rs7815788(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position56266461
is asnp
is mentioned by
dbSNPrs7815788
ebirs7815788
HLIrs7815788
Exacrs7815788
Varsomers7815788
Maprs7815788
PheGenIrs7815788
hapmaprs7815788
1000 genomesrs7815788
hgdprs7815788
ensemblrs7815788
gopubmedrs7815788
geneviewrs7815788
scholarrs7815788
googlers7815788
pharmgkbrs7815788
gwascentralrs7815788
openSNPrs7815788
23andMers7815788
23andMe allrs7815788
SNP Nexus

SNPshotrs7815788
SNPdbers7815788
MSV3drs7815788
GWAS Ctlgrs7815788
GMAF0.1442
Max Magnitude
? (C;C) (C;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 0.000005
Odds Ratio



[PMID 20027299OA-icon.png] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.


GET Evidence
rs7815788
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary