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rs9838238

From SNPedia

Orientationplus
Stabilizedplus
Make rs9838238(C;C)
Make rs9838238(C;T)
Make rs9838238(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position98881541
GeneDCBLD2
is asnp
is mentioned by
dbSNPrs9838238
dbSNP (classic)rs9838238
ClinGenrs9838238
ebirs9838238
HLIrs9838238
Exacrs9838238
Gnomadrs9838238
Varsomers9838238
LitVarrs9838238
Maprs9838238
PheGenIrs9838238
Biobankrs9838238
1000 genomesrs9838238
hgdprs9838238
ensemblrs9838238
geneviewrs9838238
scholarrs9838238
googlers9838238
pharmgkbrs9838238
gwascentralrs9838238
openSNPrs9838238
23andMers9838238
23andMe allrs9838238
SNPshotrs9838238
SNPdbers9838238
MSV3drs9838238
GWAS Ctlgrs9838238
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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