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rs3118914

From SNPedia

Orientationplus
Stabilizedplus
Make rs3118914(G;G)
Make rs3118914(G;T)
Make rs3118914(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position50542765
is asnp
is mentioned by
dbSNPrs3118914
ebirs3118914
HLIrs3118914
Exacrs3118914
Varsomers3118914
Maprs3118914
PheGenIrs3118914
hapmaprs3118914
1000 genomesrs3118914
hgdprs3118914
ensemblrs3118914
gopubmedrs3118914
geneviewrs3118914
scholarrs3118914
googlers3118914
pharmgkbrs3118914
gwascentralrs3118914
openSNPrs3118914
23andMers3118914
23andMe allrs3118914
SNP Nexus

SNPshotrs3118914
SNPdbers3118914
MSV3drs3118914
GWAS Ctlgrs3118914
GMAF0.1061
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 4E-10
Odds Ratio


OMIM612894
Desc
Variant
Relatedalso


GET Evidence
rs3118914
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.117188
summary