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

rs921122

From SNPedia

Orientationplus
Stabilizedplus
Make rs921122(C;C)
Make rs921122(C;T)
Make rs921122(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position92301665
GeneNOL8
is asnp
is mentioned by
dbSNPrs921122
dbSNP (classic)rs921122
ClinGenrs921122
ebirs921122
HLIrs921122
Exacrs921122
Gnomadrs921122
Varsomers921122
LitVarrs921122
Maprs921122
PheGenIrs921122
Biobankrs921122
1000 genomesrs921122
hgdprs921122
ensemblrs921122
geneviewrs921122
scholarrs921122
googlers921122
pharmgkbrs921122
gwascentralrs921122
openSNPrs921122
23andMers921122
23andMe allrs921122
SNPshotrs921122
SNPdbers921122
MSV3drs921122
GWAS Ctlgrs921122
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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