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rs267606657

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606657(G;G)
Make rs267606657(G;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position14741837
GeneANKH
is asnp
is mentioned by
dbSNPrs267606657
ebirs267606657
HLIrs267606657
Exacrs267606657
Varsomers267606657
Maprs267606657
PheGenIrs267606657
hapmaprs267606657
1000 genomesrs267606657
hgdprs267606657
ensemblrs267606657
gopubmedrs267606657
geneviewrs267606657
scholarrs267606657
googlers267606657
pharmgkbrs267606657
gwascentralrs267606657
openSNPrs267606657
23andMers267606657
23andMe allrs267606657
SNP Nexus

SNPshotrs267606657
SNPdbers267606657
MSV3drs267606657
GWAS Ctlgrs267606657
Max Magnitude0
ClinVar
Risk rs267606657(G;G)
Alt rs267606657(G;G)
Reference rs267606657(T;T)
Significance Pathogenic
Disease Craniometaphyseal dysplasia
Variation info
Gene ANKH
CLNDBN Craniometaphyseal dysplasia, autosomal dominant
Reversed 1
HGVS NC_000005.9:g.14741946A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005512.2,