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rs267606679

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606679(C;C)
Make rs267606679(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position61957454
GeneBEST1
is asnp
is mentioned by
dbSNPrs267606679
ebirs267606679
HLIrs267606679
Exacrs267606679
Varsomers267606679
Maprs267606679
PheGenIrs267606679
hapmaprs267606679
1000 genomesrs267606679
hgdprs267606679
ensemblrs267606679
gopubmedrs267606679
geneviewrs267606679
scholarrs267606679
googlers267606679
pharmgkbrs267606679
gwascentralrs267606679
openSNPrs267606679
23andMers267606679
23andMe allrs267606679
SNP Nexus

SNPshotrs267606679
SNPdbers267606679
MSV3drs267606679
GWAS Ctlgrs267606679
Max Magnitude0
ClinVar
Risk rs267606679(C;C)
Alt rs267606679(C;C)
Reference rs267606679(T;T)
Significance Pathogenic
Disease Vitreoretinochoroidopathy dominant
Variation info
Gene BEST1
CLNDBN Vitreoretinochoroidopathy dominant
Reversed 0
HGVS NC_000011.9:g.61724926T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002876.3,