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rs672601356

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs672601356(-;-)
Make rs672601356(-;CA)
Make rs672601356(CA;CA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position61955127
GeneBEST1
is asnp
is mentioned by
dbSNPrs672601356
ebirs672601356
HLIrs672601356
Exacrs672601356
Varsomers672601356
Maprs672601356
PheGenIrs672601356
hapmaprs672601356
1000 genomesrs672601356
hgdprs672601356
ensemblrs672601356
gopubmedrs672601356
geneviewrs672601356
scholarrs672601356
googlers672601356
pharmgkbrs672601356
gwascentralrs672601356
openSNPrs672601356
23andMers672601356
23andMe allrs672601356
SNP Nexus

SNPshotrs672601356
SNPdbers672601356
MSV3drs672601356
GWAS Ctlgrs672601356
Max Magnitude0
ClinVar
Risk rs672601356(AC;AC)
Alt rs672601356(AC;AC)
Reference rs672601356(;)
Significance Pathogenic
Disease Vitelliform dystrophy
Variation info
Gene BEST1
CLNDBN Vitelliform dystrophy
Reversed 0
HGVS NC_000011.9:g.61722598_61722599dupCA
CLNSRC
CLNACC RCV000149459.1,