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rs4345115

From SNPedia

Orientationplus
Stabilizedplus
Make rs4345115(C;C)
Make rs4345115(C;T)
Make rs4345115(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position168119960
is asnp
is mentioned by
dbSNPrs4345115
ebirs4345115
HLIrs4345115
Exacrs4345115
Varsomers4345115
Maprs4345115
PheGenIrs4345115
hapmaprs4345115
1000 genomesrs4345115
hgdprs4345115
ensemblrs4345115
gopubmedrs4345115
geneviewrs4345115
scholarrs4345115
googlers4345115
pharmgkbrs4345115
gwascentralrs4345115
openSNPrs4345115
23andMers4345115
23andMe allrs4345115
SNP Nexus

SNPshotrs4345115
SNPdbers4345115
MSV3drs4345115
GWAS Ctlgrs4345115
GMAF0.388
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele T
P-val 0.0000069999999999999999
Odds Ratio 4.40 [2.44-6.36] % SD taller


GET Evidence
rs4345115
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.288136
summary