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rs121918289

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918289(A;A)
Make rs121918289(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position61955726
GeneBEST1
is asnp
is mentioned by
dbSNPrs121918289
ebirs121918289
HLIrs121918289
Exacrs121918289
Varsomers121918289
Maprs121918289
PheGenIrs121918289
hapmaprs121918289
1000 genomesrs121918289
hgdprs121918289
ensemblrs121918289
gopubmedrs121918289
geneviewrs121918289
scholarrs121918289
googlers121918289
pharmgkbrs121918289
gwascentralrs121918289
openSNPrs121918289
23andMers121918289
23andMe allrs121918289
SNP Nexus

SNPshotrs121918289
SNPdbers121918289
MSV3drs121918289
GWAS Ctlgrs121918289
Max Magnitude0
OMIM607854
Desc
Variant0019
Relatedalso
ClinVar
Risk rs121918289(A;A)
Alt rs121918289(A;A)
Reference rs121918289(G;G)
Significance Pathogenic
Disease Vitreoretinochoroidopathy dominant
Variation info
Gene BEST1
CLNDBN Vitreoretinochoroidopathy dominant
Reversed 0
HGVS NC_000011.9:g.61723198G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002867.3,