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rs34838342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs34838342(C;C)
Make rs34838342(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position42565884
GeneGHR
is asnp
is mentioned by
dbSNPrs34838342
ebirs34838342
HLIrs34838342
Exacrs34838342
Varsomers34838342
Maprs34838342
PheGenIrs34838342
hapmaprs34838342
1000 genomesrs34838342
hgdprs34838342
ensemblrs34838342
gopubmedrs34838342
geneviewrs34838342
scholarrs34838342
googlers34838342
pharmgkbrs34838342
gwascentralrs34838342
openSNPrs34838342
23andMers34838342
23andMe allrs34838342
SNP Nexus

SNPshotrs34838342
SNPdbers34838342
MSV3drs34838342
GWAS Ctlgrs34838342
Max Magnitude0
Venter snp
Source plos
Gene GHR
allele C
frequency
sift TOLERATED
HuRef 1103654086484
Disease Association Defects in GHR are a cause of idiopathic short stature (ISS) (MIM:600946). ISS is defined by a subnormal rate of growth.