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rs267606843

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606843(A;A)
Make rs267606843(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position172448408
GeneGHSR
is asnp
is mentioned by
dbSNPrs267606843
ebirs267606843
HLIrs267606843
Exacrs267606843
Varsomers267606843
Maprs267606843
PheGenIrs267606843
hapmaprs267606843
1000 genomesrs267606843
hgdprs267606843
ensemblrs267606843
gopubmedrs267606843
geneviewrs267606843
scholarrs267606843
googlers267606843
pharmgkbrs267606843
gwascentralrs267606843
openSNPrs267606843
23andMers267606843
23andMe allrs267606843
SNP Nexus

SNPshotrs267606843
SNPdbers267606843
MSV3drs267606843
GWAS Ctlgrs267606843
Max Magnitude0
ClinVar
Risk rs267606843(A;A)
Alt rs267606843(A;A)
Reference rs267606843(G;G)
Significance Pathogenic
Disease Short stature
Variation info
Gene GHSR
CLNDBN Short stature, idiopathic, autosomal
Reversed 1
HGVS NC_000003.11:g.172166198C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008072.3,