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rs267606678

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606678(C;G)
Make rs267606678(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position61955888
GeneBEST1
is asnp
is mentioned by
dbSNPrs267606678
ebirs267606678
HLIrs267606678
Exacrs267606678
Varsomers267606678
Maprs267606678
PheGenIrs267606678
hapmaprs267606678
1000 genomesrs267606678
hgdprs267606678
ensemblrs267606678
gopubmedrs267606678
geneviewrs267606678
scholarrs267606678
googlers267606678
pharmgkbrs267606678
gwascentralrs267606678
openSNPrs267606678
23andMers267606678
23andMe allrs267606678
SNP Nexus

SNPshotrs267606678
SNPdbers267606678
MSV3drs267606678
GWAS Ctlgrs267606678
Max Magnitude0
ClinVar
Risk rs267606678(G;G)
Alt rs267606678(G;G)
Reference rs267606678(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 50
Variation info
Gene BEST1
CLNDBN Retinitis pigmentosa 50
Reversed 0
HGVS NC_000011.9:g.61723360C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002875.3,