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rs34815962

From SNPedia

Orientationplus
Stabilizedplus
Make rs34815962(C;C)
Make rs34815962(C;T)
Make rs34815962(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position72169914
GeneGRAMD2
is asnp
is mentioned by
dbSNPrs34815962
dbSNP (classic)rs34815962
ClinGenrs34815962
ebirs34815962
HLIrs34815962
Exacrs34815962
Gnomadrs34815962
Varsomers34815962
LitVarrs34815962
Maprs34815962
PheGenIrs34815962
Biobankrs34815962
1000 genomesrs34815962
hgdprs34815962
ensemblrs34815962
geneviewrs34815962
scholarrs34815962
googlers34815962
pharmgkbrs34815962
gwascentralrs34815962
openSNPrs34815962
23andMers34815962
23andMe allrs34815962
SNPshotrs34815962
SNPdbers34815962
MSV3drs34815962
GWAS Ctlgrs34815962
Max Magnitude0

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