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rs786204762

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204762(A;A)
Make rs786204762(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position86643810
GeneCNGB3
is asnp
is mentioned by
dbSNPrs786204762
ebirs786204762
HLIrs786204762
Exacrs786204762
Varsomers786204762
Maprs786204762
PheGenIrs786204762
hapmaprs786204762
1000 genomesrs786204762
hgdprs786204762
ensemblrs786204762
gopubmedrs786204762
geneviewrs786204762
scholarrs786204762
googlers786204762
pharmgkbrs786204762
gwascentralrs786204762
openSNPrs786204762
23andMers786204762
23andMe allrs786204762
SNP Nexus

SNPshotrs786204762
SNPdbers786204762
MSV3drs786204762
GWAS Ctlgrs786204762
Max Magnitude0
ClinVar
Risk rs786204762(A;A)
Alt rs786204762(A;A)
Reference rs786204762(G;G)
Significance Probable-Pathogenic
Disease Achromatopsia 3
Variation info
Gene CNGB3
CLNDBN Achromatopsia 3
Reversed 1
HGVS NC_000008.10:g.87656038C>T
CLNSRC
CLNACC RCV000169624.1,