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rs61733564

From SNPedia

Orientationplus
Stabilizedplus
Make rs61733564(A;A)
Make rs61733564(A;G)
Make rs61733564(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position4762704
GeneZNF500
is asnp
is mentioned by
dbSNPrs61733564
dbSNP (classic)rs61733564
ClinGenrs61733564
ebirs61733564
HLIrs61733564
Exacrs61733564
Gnomadrs61733564
Varsomers61733564
LitVarrs61733564
Maprs61733564
PheGenIrs61733564
Biobankrs61733564
1000 genomesrs61733564
hgdprs61733564
ensemblrs61733564
geneviewrs61733564
scholarrs61733564
googlers61733564
pharmgkbrs61733564
gwascentralrs61733564
openSNPrs61733564
23andMers61733564
23andMe allrs61733564
SNPshotrs61733564
SNPdbers61733564
MSV3drs61733564
GWAS Ctlgrs61733564
Max Magnitude0

[PMID 28146470OA-icon.png] Rare and low-frequency coding variants alter human adult height.