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rs1064794342

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACGA;ACGA) 0 common in clinvar
Chromosome16
Position57903851
GeneCNGB1
is asnp
is mentioned by
dbSNPrs1064794342
dbSNP (old)rs1064794342
ClinGenrs1064794342
ebirs1064794342
HLIrs1064794342
Exacrs1064794342
Gnomadrs1064794342
Varsomers1064794342
LitVarrs1064794342
Maprs1064794342
PheGenIrs1064794342
Biobankrs1064794342
1000 genomesrs1064794342
hgdprs1064794342
ensemblrs1064794342
gopubmedrs1064794342
geneviewrs1064794342
scholarrs1064794342
googlers1064794342
pharmgkbrs1064794342
gwascentralrs1064794342
openSNPrs1064794342
23andMers1064794342
23andMe allrs1064794342
SNPshotrs1064794342
SNPdbers1064794342
MSV3drs1064794342
GWAS Ctlgrs1064794342
Max Magnitude0
ClinVar
Risk rs1064794342(-;-)
Alt rs1064794342(-;-)
Reference Rs1064794342(ACGA;ACGA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CNGB1
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.57937755_57937758delTCGT
CLNSRC
CLNACC RCV000479018.1,