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rs267606733

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606733(C;T)
Make rs267606733(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position72007512
GeneCHST3
is asnp
is mentioned by
dbSNPrs267606733
ebirs267606733
HLIrs267606733
Exacrs267606733
Varsomers267606733
Maprs267606733
PheGenIrs267606733
hapmaprs267606733
1000 genomesrs267606733
hgdprs267606733
ensemblrs267606733
gopubmedrs267606733
geneviewrs267606733
scholarrs267606733
googlers267606733
pharmgkbrs267606733
gwascentralrs267606733
openSNPrs267606733
23andMers267606733
23andMe allrs267606733
SNP Nexus

SNPshotrs267606733
SNPdbers267606733
MSV3drs267606733
GWAS Ctlgrs267606733
Max Magnitude0
ClinVar
Risk rs267606733(T;T)
Alt rs267606733(T;T)
Reference rs267606733(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.73767270C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006422.3,