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rs267606735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606735(C;T)
Make rs267606735(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position72007453
GeneCHST3
is asnp
is mentioned by
dbSNPrs267606735
ebirs267606735
HLIrs267606735
Exacrs267606735
Varsomers267606735
Maprs267606735
PheGenIrs267606735
hapmaprs267606735
1000 genomesrs267606735
hgdprs267606735
ensemblrs267606735
gopubmedrs267606735
geneviewrs267606735
scholarrs267606735
googlers267606735
pharmgkbrs267606735
gwascentralrs267606735
openSNPrs267606735
23andMers267606735
23andMe allrs267606735
SNP Nexus

SNPshotrs267606735
SNPdbers267606735
MSV3drs267606735
GWAS Ctlgrs267606735
Max Magnitude0
ClinVar
Risk rs267606735(A,T;A,T)
Alt rs267606735(A,T;A,T)
Reference rs267606735(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.73767211C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006420.4,