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rs267606680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606680(C;C)
Make rs267606680(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position61956976
GeneBEST1
is asnp
is mentioned by
dbSNPrs267606680
ebirs267606680
HLIrs267606680
Exacrs267606680
Varsomers267606680
Maprs267606680
PheGenIrs267606680
hapmaprs267606680
1000 genomesrs267606680
hgdprs267606680
ensemblrs267606680
gopubmedrs267606680
geneviewrs267606680
scholarrs267606680
googlers267606680
pharmgkbrs267606680
gwascentralrs267606680
openSNPrs267606680
23andMers267606680
23andMe allrs267606680
SNP Nexus

SNPshotrs267606680
SNPdbers267606680
MSV3drs267606680
GWAS Ctlgrs267606680
Max Magnitude0
ClinVar
Risk rs267606680(C;C)
Alt rs267606680(C;C)
Reference rs267606680(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 50
Variation info
Gene BEST1
CLNDBN Retinitis pigmentosa 50
Reversed 0
HGVS NC_000011.9:g.61724448T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002870.3,