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rs147346345

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147346345(A;A)
Make rs147346345(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position84203123
GeneCDHR1
is asnp
is mentioned by
dbSNPrs147346345
dbSNP (classic)rs147346345
ClinGenrs147346345
ebirs147346345
HLIrs147346345
Exacrs147346345
Gnomadrs147346345
Varsomers147346345
LitVarrs147346345
Maprs147346345
PheGenIrs147346345
Biobankrs147346345
1000 genomesrs147346345
hgdprs147346345
ensemblrs147346345
geneviewrs147346345
scholarrs147346345
googlers147346345
pharmgkbrs147346345
gwascentralrs147346345
openSNPrs147346345
23andMers147346345
23andMe allrs147346345
SNPshotrs147346345
SNPdbers147346345
MSV3drs147346345
GWAS Ctlgrs147346345
Max Magnitude0
ClinVar
Risk rs147346345(A;A) rs147346345(C;C)
Alt rs147346345(A;A) rs147346345(C;C)
Reference Rs147346345(G;G)
Significance Probable-Pathogenic
Disease Cone-Rod Dystrophy not provided
Variation info
Gene CDHR1
CLNDBN Cone-Rod Dystrophy, Recessive not provided
Reversed 0
HGVS NC_000010.10:g.85962879G>A
CLNSRC
CLNACC RCV000369498.1, RCV000487554.1,