Have questions? Visit https://www.reddit.com/r/SNPedia

rs7689420

From SNPedia

Orientationplus
Stabilizedplus
Make rs7689420(C;C)
Make rs7689420(C;T)
Make rs7689420(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position144647200
GeneHHIP, TTTY18
is asnp
is mentioned by
dbSNPrs7689420
ebirs7689420
HLIrs7689420
Exacrs7689420
Varsomers7689420
Maprs7689420
PheGenIrs7689420
hapmaprs7689420
1000 genomesrs7689420
hgdprs7689420
ensemblrs7689420
gopubmedrs7689420
geneviewrs7689420
scholarrs7689420
googlers7689420
pharmgkbrs7689420
gwascentralrs7689420
openSNPrs7689420
23andMers7689420
23andMe allrs7689420
SNP Nexus

SNPshotrs7689420
SNPdbers7689420
MSV3drs7689420
GWAS Ctlgrs7689420
GMAF0.2571
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 6E-51
Odds Ratio .07 [NR] unit decrease
GWAS snp
PMID [PMID 23563607OA-icon.png]
Trait Height
Title Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Risk Allele C
P-val 4E-21
Odds Ratio 1.33 [NR]