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rs199588904

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199588904(A;A)
Make rs199588904(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position172447705
GeneGHSR
is asnp
is mentioned by
dbSNPrs199588904
ebirs199588904
HLIrs199588904
Exacrs199588904
Varsomers199588904
Maprs199588904
PheGenIrs199588904
hapmaprs199588904
1000 genomesrs199588904
hgdprs199588904
ensemblrs199588904
gopubmedrs199588904
geneviewrs199588904
scholarrs199588904
googlers199588904
pharmgkbrs199588904
gwascentralrs199588904
openSNPrs199588904
23andMers199588904
23andMe allrs199588904
SNP Nexus

SNPshotrs199588904
SNPdbers199588904
MSV3drs199588904
GWAS Ctlgrs199588904
Max Magnitude0
ClinVar
Risk rs199588904(A;A)
Alt rs199588904(A;A)
Reference rs199588904(T;T)
Significance Pathogenic
Disease Short stature
Variation info
Gene GHSR
CLNDBN Short stature, idiopathic, autosomal
Reversed 0
HGVS NC_000003.11:g.172165495T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008073.4,