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rs193922466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922466(A;G)
Make rs193922466(G;G)
ReferenceGRCh38 38.1/141
ChromosomeY
Position634687
GeneSHOX
is asnp
is mentioned by
dbSNPrs193922466
ebirs193922466
HLIrs193922466
Exacrs193922466
Varsomers193922466
Maprs193922466
PheGenIrs193922466
hapmaprs193922466
1000 genomesrs193922466
hgdprs193922466
ensemblrs193922466
gopubmedrs193922466
geneviewrs193922466
scholarrs193922466
googlers193922466
pharmgkbrs193922466
gwascentralrs193922466
openSNPrs193922466
23andMers193922466
23andMe allrs193922466
SNP Nexus

SNPshotrs193922466
SNPdbers193922466
MSV3drs193922466
GWAS Ctlgrs193922466
Y Chromrs193922466
Max Magnitude0
ClinVar
Risk rs193922466(G;G)
Alt rs193922466(G;G)
Reference rs193922466(A;A)
Significance Probable-Pathogenic
Disease Short stature
Variation info
Gene SHOX
CLNDBN Short stature, idiopathic, X-linked
Reversed 0
HGVS NC_000023.10:g.595422A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030453.1,