Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606702

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606702(A;A)
Make rs267606702(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position78997249
GeneCANT1
is asnp
is mentioned by
dbSNPrs267606702
ebirs267606702
HLIrs267606702
Exacrs267606702
Varsomers267606702
Maprs267606702
PheGenIrs267606702
hapmaprs267606702
1000 genomesrs267606702
hgdprs267606702
ensemblrs267606702
gopubmedrs267606702
geneviewrs267606702
scholarrs267606702
googlers267606702
pharmgkbrs267606702
gwascentralrs267606702
openSNPrs267606702
23andMers267606702
23andMe allrs267606702
SNP Nexus

SNPshotrs267606702
SNPdbers267606702
MSV3drs267606702
GWAS Ctlgrs267606702
Max Magnitude0
ClinVar
Risk rs267606702(A;A)
Alt rs267606702(A;A)
Reference rs267606702(G;G)
Significance Pathogenic
Disease Desbuquois syndrome
Variation info
Gene CANT1
CLNDBN Desbuquois syndrome
Reversed 1
HGVS NC_000017.10:g.76993331C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000306.4,