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rs1064796793

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position86611587
GeneCNGB3
is asnp
is mentioned by
dbSNPrs1064796793
dbSNP (classic)rs1064796793
ClinGenrs1064796793
ebirs1064796793
HLIrs1064796793
Exacrs1064796793
Gnomadrs1064796793
Varsomers1064796793
LitVarrs1064796793
Maprs1064796793
PheGenIrs1064796793
Biobankrs1064796793
1000 genomesrs1064796793
hgdprs1064796793
ensemblrs1064796793
geneviewrs1064796793
scholarrs1064796793
googlers1064796793
pharmgkbrs1064796793
gwascentralrs1064796793
openSNPrs1064796793
23andMers1064796793
23andMe allrs1064796793
SNPshotrs1064796793
SNPdbers1064796793
MSV3drs1064796793
GWAS Ctlgrs1064796793
Max Magnitude0
ClinVar
Risk rs1064796793(A;A)
Alt rs1064796793(A;A)
Reference Rs1064796793(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CNGB3
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.87623815C>T
CLNSRC
CLNACC RCV000485915.1,