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rs117295933

From SNPedia

Orientationplus
Stabilizedplus
Make rs117295933(A;A)
Make rs117295933(A;C)
Make rs117295933(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position44934496
GeneKLHL28
is asnp
is mentioned by
dbSNPrs117295933
dbSNP (old)rs117295933
ClinGenrs117295933
ebirs117295933
HLIrs117295933
Exacrs117295933
Gnomadrs117295933
Varsomers117295933
Maprs117295933
PheGenIrs117295933
Biobankrs117295933
1000 genomesrs117295933
hgdprs117295933
ensemblrs117295933
gopubmedrs117295933
geneviewrs117295933
scholarrs117295933
googlers117295933
pharmgkbrs117295933
gwascentralrs117295933
openSNPrs117295933
23andMers117295933
23andMe allrs117295933
SNPshotrs117295933
SNPdbers117295933
MSV3drs117295933
GWAS Ctlgrs117295933
Max Magnitude

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