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rs886043634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position634780
GeneSHOX
is asnp
is mentioned by
dbSNPrs886043634
dbSNP (classic)rs886043634
ClinGenrs886043634
ebirs886043634
HLIrs886043634
Exacrs886043634
Gnomadrs886043634
Varsomers886043634
LitVarrs886043634
Maprs886043634
PheGenIrs886043634
Biobankrs886043634
1000 genomesrs886043634
hgdprs886043634
ensemblrs886043634
geneviewrs886043634
scholarrs886043634
googlers886043634
pharmgkbrs886043634
gwascentralrs886043634
openSNPrs886043634
23andMers886043634
SNPshotrs886043634
SNPdbers886043634
MSV3drs886043634
GWAS Ctlgrs886043634
Max Magnitude0
ClinVar
Risk rs886043634(A;A)
Alt rs886043634(A;A)
Reference Rs886043634(G;G)
Significance Pathogenic
Disease Leri Weill dyschondrosteosis Short stature
Variation info
Gene SHOX
CLNDBN Leri Weill dyschondrosteosis Short stature, idiopathic, X-linked
Reversed 0
HGVS NC_000023.10:g.595515G>A
CLNSRC
CLNACC RCV000277379.1, RCV000369436.1,