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rs77885044

From SNPedia

Orientationplus
Stabilizedplus
Make rs77885044(C;C)
Make rs77885044(C;T)
Make rs77885044(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome22
Position28105426
GeneTTC28
is asnp
is mentioned by
dbSNPrs77885044
dbSNP (classic)rs77885044
ClinGenrs77885044
ebirs77885044
HLIrs77885044
Exacrs77885044
Gnomadrs77885044
Varsomers77885044
LitVarrs77885044
Maprs77885044
PheGenIrs77885044
Biobankrs77885044
1000 genomesrs77885044
hgdprs77885044
ensemblrs77885044
geneviewrs77885044
scholarrs77885044
googlers77885044
pharmgkbrs77885044
gwascentralrs77885044
openSNPrs77885044
23andMers77885044
23andMe allrs77885044
SNPshotrs77885044
SNPdbers77885044
MSV3drs77885044
GWAS Ctlgrs77885044
Max Magnitude0

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