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

rs863223306

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223306(A;A)
Make rs863223306(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position63917989
GeneGH1
is asnp
is mentioned by
dbSNPrs863223306
ebirs863223306
HLIrs863223306
Exacrs863223306
Varsomers863223306
Maprs863223306
PheGenIrs863223306
hapmaprs863223306
1000 genomesrs863223306
hgdprs863223306
ensemblrs863223306
gopubmedrs863223306
geneviewrs863223306
scholarrs863223306
googlers863223306
pharmgkbrs863223306
gwascentralrs863223306
openSNPrs863223306
23andMers863223306
23andMe allrs863223306
SNP Nexus

SNPshotrs863223306
SNPdbers863223306
MSV3drs863223306
GWAS Ctlgrs863223306
Max Magnitude0
ClinVar
Risk rs863223306(A;A)
Alt rs863223306(A;A)
Reference rs863223306(G;G)
Significance Pathogenic
Disease Autosomal dominant isolated somatotropin deficiency
Variation info
Gene GH1
CLNDBN Autosomal dominant isolated somatotropin deficiency
Reversed 1
HGVS NC_000017.10:g.61995349C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017342.26,