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rs117801489

From SNPedia
Orientationplus
Stabilizedplus
Make rs117801489(C;C)
Make rs117801489(C;T)
Make rs117801489(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position104015054
GeneGLT8D2
is asnp
is mentioned by
dbSNPrs117801489
dbSNP (old)rs117801489
ClinGenrs117801489
ebirs117801489
HLIrs117801489
Exacrs117801489
Gnomadrs117801489
Varsomers117801489
Maprs117801489
PheGenIrs117801489
Biobankrs117801489
1000 genomesrs117801489
hgdprs117801489
ensemblrs117801489
gopubmedrs117801489
geneviewrs117801489
scholarrs117801489
googlers117801489
pharmgkbrs117801489
gwascentralrs117801489
openSNPrs117801489
23andMers117801489
23andMe allrs117801489
SNPshotrs117801489
SNPdbers117801489
MSV3drs117801489
GWAS Ctlgrs117801489
Max Magnitude

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