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rs768345097

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768345097(A;A)
Make rs768345097(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position86667131
GeneCNGB3
is asnp
is mentioned by
dbSNPrs768345097
ebirs768345097
HLIrs768345097
Exacrs768345097
Varsomers768345097
Maprs768345097
PheGenIrs768345097
hapmaprs768345097
1000 genomesrs768345097
hgdprs768345097
ensemblrs768345097
gopubmedrs768345097
geneviewrs768345097
scholarrs768345097
googlers768345097
pharmgkbrs768345097
gwascentralrs768345097
openSNPrs768345097
23andMers768345097
23andMe allrs768345097
SNP Nexus

SNPshotrs768345097
SNPdbers768345097
MSV3drs768345097
GWAS Ctlgrs768345097
Max Magnitude0
ClinVar
Risk rs768345097(A;A)
Alt rs768345097(A;A)
Reference rs768345097(G;G)
Significance Probable-Pathogenic
Disease Achromatopsia 3
Variation info
Gene CNGB3
CLNDBN Achromatopsia 3
Reversed 0
HGVS NC_000008.10:g.87679359G>A
CLNSRC
CLNACC RCV000169194.1,