Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909362

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909362(C;T)
Make rs121909362(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position42699919
GeneGHR
is asnp
is mentioned by
dbSNPrs121909362
ebirs121909362
HLIrs121909362
Exacrs121909362
Varsomers121909362
Maprs121909362
PheGenIrs121909362
hapmaprs121909362
1000 genomesrs121909362
hgdprs121909362
ensemblrs121909362
gopubmedrs121909362
geneviewrs121909362
scholarrs121909362
googlers121909362
pharmgkbrs121909362
gwascentralrs121909362
openSNPrs121909362
23andMers121909362
23andMe allrs121909362
SNP Nexus

SNPshotrs121909362
SNPdbers121909362
MSV3drs121909362
GWAS Ctlgrs121909362
GMAF0.002296
Max Magnitude0
OMIM600946
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909362(T;T)
Alt rs121909362(T;T)
Reference rs121909362(C;C)
Significance Pathogenic
Disease Short stature not provided
Variation info
Gene GHR
CLNDBN Short stature, idiopathic, autosomal not provided
Reversed 0
HGVS NC_000005.9:g.42700021C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009169.3, RCV000179265.1,