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rs863224862

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224862(C;C)
Make rs863224862(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position197427552
GeneCRB1
is asnp
is mentioned by
dbSNPrs863224862
ebirs863224862
HLIrs863224862
Exacrs863224862
Varsomers863224862
Maprs863224862
PheGenIrs863224862
hapmaprs863224862
1000 genomesrs863224862
hgdprs863224862
ensemblrs863224862
gopubmedrs863224862
geneviewrs863224862
scholarrs863224862
googlers863224862
pharmgkbrs863224862
gwascentralrs863224862
openSNPrs863224862
23andMers863224862
23andMe allrs863224862
SNP Nexus

SNPshotrs863224862
SNPdbers863224862
MSV3drs863224862
GWAS Ctlgrs863224862
Max Magnitude0
ClinVar
Risk rs863224862(C;C)
Alt rs863224862(C;C)
Reference rs863224862(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa 12
Variation info
Gene CRB1
CLNDBN Retinitis pigmentosa 12
Reversed 0
HGVS NC_000001.10:g.197396682G>C
CLNSRC
CLNACC RCV000199723.1,