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rs267606699

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606699(A;A)
Make rs267606699(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position78993857
GeneCANT1
is asnp
is mentioned by
dbSNPrs267606699
ebirs267606699
HLIrs267606699
Exacrs267606699
Varsomers267606699
Maprs267606699
PheGenIrs267606699
hapmaprs267606699
1000 genomesrs267606699
hgdprs267606699
ensemblrs267606699
gopubmedrs267606699
geneviewrs267606699
scholarrs267606699
googlers267606699
pharmgkbrs267606699
gwascentralrs267606699
openSNPrs267606699
23andMers267606699
23andMe allrs267606699
SNP Nexus

SNPshotrs267606699
SNPdbers267606699
MSV3drs267606699
GWAS Ctlgrs267606699
Max Magnitude0
ClinVar
Risk rs267606699(A;A)
Alt rs267606699(A;A)
Reference rs267606699(G;G)
Significance Pathogenic
Disease Desbuquois syndrome
Variation info
Gene CANT1
CLNDBN Desbuquois syndrome
Reversed 1
HGVS NC_000017.10:g.76989939C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000304.3,