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

rs267606739

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606739(C;T)
Make rs267606739(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position86668055
GeneCNGB3
is asnp
is mentioned by
dbSNPrs267606739
ebirs267606739
HLIrs267606739
Exacrs267606739
Varsomers267606739
Maprs267606739
PheGenIrs267606739
hapmaprs267606739
1000 genomesrs267606739
hgdprs267606739
ensemblrs267606739
gopubmedrs267606739
geneviewrs267606739
scholarrs267606739
googlers267606739
pharmgkbrs267606739
gwascentralrs267606739
openSNPrs267606739
23andMers267606739
23andMe allrs267606739
SNP Nexus

SNPshotrs267606739
SNPdbers267606739
MSV3drs267606739
GWAS Ctlgrs267606739
Max Magnitude0
ClinVar
Risk rs267606739(G,T;G,T)
Alt rs267606739(G,T;G,T)
Reference rs267606739(C;C)
Significance Other
Disease Achromatopsia 3
Variation info
Gene CNGB3
CLNDBN Achromatopsia 3
Reversed 1
HGVS NC_000008.10:g.87680283G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005533.4,