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rs116858574

From SNPedia

Orientationplus
Stabilizedplus
Make rs116858574(C;C)
Make rs116858574(C;T)
Make rs116858574(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position34228486
GeneEMC4
is asnp
is mentioned by
dbSNPrs116858574
dbSNP (old)rs116858574
ClinGenrs116858574
ebirs116858574
HLIrs116858574
Exacrs116858574
Gnomadrs116858574
Varsomers116858574
LitVarrs116858574
Maprs116858574
PheGenIrs116858574
Biobankrs116858574
1000 genomesrs116858574
hgdprs116858574
ensemblrs116858574
gopubmedrs116858574
geneviewrs116858574
scholarrs116858574
googlers116858574
pharmgkbrs116858574
gwascentralrs116858574
openSNPrs116858574
23andMers116858574
23andMe allrs116858574
SNPshotrs116858574
SNPdbers116858574
MSV3drs116858574
GWAS Ctlgrs116858574
Max Magnitude

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