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rs121918291

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918291(A;G)
Make rs121918291(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position61957457
GeneBEST1
is asnp
is mentioned by
dbSNPrs121918291
ebirs121918291
HLIrs121918291
Exacrs121918291
Varsomers121918291
Maprs121918291
PheGenIrs121918291
hapmaprs121918291
1000 genomesrs121918291
hgdprs121918291
ensemblrs121918291
gopubmedrs121918291
geneviewrs121918291
scholarrs121918291
googlers121918291
pharmgkbrs121918291
gwascentralrs121918291
openSNPrs121918291
23andMers121918291
23andMe allrs121918291
SNP Nexus

SNPshotrs121918291
SNPdbers121918291
MSV3drs121918291
GWAS Ctlgrs121918291
Max Magnitude0
OMIM607854
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121918291(G;G)
Alt rs121918291(G;G)
Reference rs121918291(A;A)
Significance Pathogenic
Disease Vitreoretinochoroidopathy dominant
Variation info
Gene BEST1
CLNDBN Vitreoretinochoroidopathy dominant
Reversed 0
HGVS NC_000011.9:g.61724929A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002869.3,