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rs7697556

From SNPedia

Orientationplus
Stabilizedplus
Make rs7697556(C;C)
Make rs7697556(C;T)
Make rs7697556(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position72649596
is asnp
is mentioned by
dbSNPrs7697556
ebirs7697556
HLIrs7697556
Exacrs7697556
Varsomers7697556
Maprs7697556
PheGenIrs7697556
hapmaprs7697556
1000 genomesrs7697556
hgdprs7697556
ensemblrs7697556
gopubmedrs7697556
geneviewrs7697556
scholarrs7697556
googlers7697556
pharmgkbrs7697556
gwascentralrs7697556
openSNPrs7697556
23andMers7697556
23andMe allrs7697556
SNP Nexus

SNPshotrs7697556
SNPdbers7697556
MSV3drs7697556
GWAS Ctlgrs7697556
GMAF0.4481
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 2E-14
Odds Ratio 0.03 [NR] unit increase