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rs267606732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606732(C;T)
Make rs267606732(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position72008019
GeneCHST3
is asnp
is mentioned by
dbSNPrs267606732
ebirs267606732
HLIrs267606732
Exacrs267606732
Varsomers267606732
Maprs267606732
PheGenIrs267606732
hapmaprs267606732
1000 genomesrs267606732
hgdprs267606732
ensemblrs267606732
gopubmedrs267606732
geneviewrs267606732
scholarrs267606732
googlers267606732
pharmgkbrs267606732
gwascentralrs267606732
openSNPrs267606732
23andMers267606732
23andMe allrs267606732
SNP Nexus

SNPshotrs267606732
SNPdbers267606732
MSV3drs267606732
GWAS Ctlgrs267606732
Max Magnitude0
ClinVar
Risk rs267606732(A,T;A,T)
Alt rs267606732(A,T;A,T)
Reference rs267606732(C;C)
Significance Pathogenic
Disease Spondyloepiphyseal dysplasia with congenital joint dislocations
Variation info
Gene CHST3
CLNDBN Spondyloepiphyseal dysplasia with congenital joint dislocations
Reversed 0
HGVS NC_000010.10:g.73767777C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006423.3,