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rs140385822

From SNPedia

Orientationplus
Stabilizedplus
Make rs140385822(A;A)
Make rs140385822(A;G)
Make rs140385822(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position67436602
GeneHSD11B2
is asnp
is mentioned by
dbSNPrs140385822
dbSNP (classic)rs140385822
ClinGenrs140385822
ebirs140385822
HLIrs140385822
Exacrs140385822
Gnomadrs140385822
Varsomers140385822
LitVarrs140385822
Maprs140385822
PheGenIrs140385822
Biobankrs140385822
1000 genomesrs140385822
hgdprs140385822
ensemblrs140385822
geneviewrs140385822
scholarrs140385822
googlers140385822
pharmgkbrs140385822
gwascentralrs140385822
openSNPrs140385822
23andMers140385822
23andMe allrs140385822
SNPshotrs140385822
SNPdbers140385822
MSV3drs140385822
GWAS Ctlgrs140385822
Max Magnitude0

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