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rs760430056

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs760430056(-;-)
Make rs760430056(-;C)
Make rs760430056(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position57904823
GeneCNGB1
is asnp
is mentioned by
dbSNPrs760430056
ebirs760430056
HLIrs760430056
Exacrs760430056
Varsomers760430056
Maprs760430056
PheGenIrs760430056
hapmaprs760430056
1000 genomesrs760430056
hgdprs760430056
ensemblrs760430056
gopubmedrs760430056
geneviewrs760430056
scholarrs760430056
googlers760430056
pharmgkbrs760430056
gwascentralrs760430056
openSNPrs760430056
23andMers760430056
23andMe allrs760430056
SNP Nexus

SNPshotrs760430056
SNPdbers760430056
MSV3drs760430056
GWAS Ctlgrs760430056
Max Magnitude0
ClinVar
Risk rs760430056(C;C)
Alt rs760430056(C;C)
Reference rs760430056(;)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CNGB1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000016.9:g.57938728dupC
CLNSRC
CLNACC RCV000225473.1,