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rs147996581

From SNPedia

Orientationplus
Stabilizedplus
Make rs147996581(A;A)
Make rs147996581(A;G)
Make rs147996581(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position57745188
GeneTSPAN31
is asnp
is mentioned by
dbSNPrs147996581
dbSNP (classic)rs147996581
ClinGenrs147996581
ebirs147996581
HLIrs147996581
Exacrs147996581
Gnomadrs147996581
Varsomers147996581
LitVarrs147996581
Maprs147996581
PheGenIrs147996581
Biobankrs147996581
1000 genomesrs147996581
hgdprs147996581
ensemblrs147996581
geneviewrs147996581
scholarrs147996581
googlers147996581
pharmgkbrs147996581
gwascentralrs147996581
openSNPrs147996581
23andMers147996581
23andMe allrs147996581
SNPshotrs147996581
SNPdbers147996581
MSV3drs147996581
GWAS Ctlgrs147996581
Max Magnitude0

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