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rs281865238

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865238(A;A)
Make rs281865238(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position61957402
GeneBEST1
is asnp
is mentioned by
dbSNPrs281865238
ebirs281865238
HLIrs281865238
Exacrs281865238
Varsomers281865238
Maprs281865238
PheGenIrs281865238
hapmaprs281865238
1000 genomesrs281865238
hgdprs281865238
ensemblrs281865238
gopubmedrs281865238
geneviewrs281865238
scholarrs281865238
googlers281865238
pharmgkbrs281865238
gwascentralrs281865238
openSNPrs281865238
23andMers281865238
23andMe allrs281865238
SNP Nexus

SNPshotrs281865238
SNPdbers281865238
MSV3drs281865238
GWAS Ctlgrs281865238
Max Magnitude0
ClinVar
Risk rs281865238(A,T;A,T)
Alt rs281865238(A,T;A,T)
Reference rs281865238(C;C)
Significance Probable-Pathogenic
Disease not provided Vitelliform dystrophy
Variation info
Gene BEST1
CLNDBN not provided Vitelliform dystrophy
Reversed 0
HGVS NC_000011.9:g.61724874C>A; NC_000011.9:g.61724874C>T
CLNSRC
CLNACC RCV000086149.1, RCV000086150.1, RCV000179430.1,