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rs71455793

From SNPedia

Orientationplus
Stabilizedplus
Make rs71455793(A;A)
Make rs71455793(A;G)
Make rs71455793(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position65947733
GeneTSGA10IP
is asnp
is mentioned by
dbSNPrs71455793
dbSNP (classic)rs71455793
ClinGenrs71455793
ebirs71455793
HLIrs71455793
Exacrs71455793
Gnomadrs71455793
Varsomers71455793
LitVarrs71455793
Maprs71455793
PheGenIrs71455793
Biobankrs71455793
1000 genomesrs71455793
hgdprs71455793
ensemblrs71455793
geneviewrs71455793
scholarrs71455793
googlers71455793
pharmgkbrs71455793
gwascentralrs71455793
openSNPrs71455793
23andMers71455793
23andMe allrs71455793
SNPshotrs71455793
SNPdbers71455793
MSV3drs71455793
GWAS Ctlgrs71455793
Max Magnitude0

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