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rs144673025

From SNPedia

Orientationplus
Stabilizedplus
Make rs144673025(C;C)
Make rs144673025(C;T)
Make rs144673025(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position223004684
GeneDISP1
is asnp
is mentioned by
dbSNPrs144673025
dbSNP (classic)rs144673025
ClinGenrs144673025
ebirs144673025
HLIrs144673025
Exacrs144673025
Gnomadrs144673025
Varsomers144673025
LitVarrs144673025
Maprs144673025
PheGenIrs144673025
Biobankrs144673025
1000 genomesrs144673025
hgdprs144673025
ensemblrs144673025
geneviewrs144673025
scholarrs144673025
googlers144673025
pharmgkbrs144673025
gwascentralrs144673025
openSNPrs144673025
23andMers144673025
23andMe allrs144673025
SNPshotrs144673025
SNPdbers144673025
MSV3drs144673025
GWAS Ctlgrs144673025
Max Magnitude0

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