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rs7178424

From SNPedia

Orientationplus
Stabilizedplus
Make rs7178424(C;C)
Make rs7178424(C;T)
Make rs7178424(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position62088060
is asnp
is mentioned by
dbSNPrs7178424
ebirs7178424
HLIrs7178424
Exacrs7178424
Varsomers7178424
Maprs7178424
PheGenIrs7178424
hapmaprs7178424
1000 genomesrs7178424
hgdprs7178424
ensemblrs7178424
gopubmedrs7178424
geneviewrs7178424
scholarrs7178424
googlers7178424
pharmgkbrs7178424
gwascentralrs7178424
openSNPrs7178424
23andMers7178424
23andMe allrs7178424
SNP Nexus

SNPshotrs7178424
SNPdbers7178424
MSV3drs7178424
GWAS Ctlgrs7178424
GMAF0.4215
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 6E-9
Odds Ratio 0.0200 [NR] meters decrease