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rs797044693

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044693(-;C)
Make rs797044693(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position57904811
GeneCNGB1
is asnp
is mentioned by
dbSNPrs797044693
ClinGenrs797044693
ebirs797044693
HLIrs797044693
Exacrs797044693
Varsomers797044693
Maprs797044693
PheGenIrs797044693
hapmaprs797044693
1000 genomesrs797044693
hgdprs797044693
ensemblrs797044693
gopubmedrs797044693
geneviewrs797044693
scholarrs797044693
googlers797044693
pharmgkbrs797044693
gwascentralrs797044693
openSNPrs797044693
23andMers797044693
23andMe allrs797044693
SNP Nexus

SNPshotrs797044693
SNPdbers797044693
MSV3drs797044693
GWAS Ctlgrs797044693
Max Magnitude0
ClinVar
Risk rs797044693(C;C)
Alt rs797044693(C;C)
Reference Rs797044693(-;-)
Significance Pathogenic
Disease Retinitis pigmentosa 45
Variation info
Gene CNGB1
CLNDBN Retinitis pigmentosa 45
Reversed 1
HGVS NC_000016.9:g.57938716dupG
CLNSRC
CLNACC RCV000176637.1,