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rs62635655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62635655(G;T)
Make rs62635655(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position197434846
GeneCRB1
is asnp
is mentioned by
dbSNPrs62635655
ebirs62635655
HLIrs62635655
Exacrs62635655
Varsomers62635655
Maprs62635655
PheGenIrs62635655
hapmaprs62635655
1000 genomesrs62635655
hgdprs62635655
ensemblrs62635655
gopubmedrs62635655
geneviewrs62635655
scholarrs62635655
googlers62635655
pharmgkbrs62635655
gwascentralrs62635655
openSNPrs62635655
23andMers62635655
23andMe allrs62635655
SNP Nexus

SNPshotrs62635655
SNPdbers62635655
MSV3drs62635655
GWAS Ctlgrs62635655
Max Magnitude0
OMIM604210
Desc
Variant0003
Relatedalso


ClinVar
Risk rs62635655(A,T;A,T)
Alt rs62635655(A,T;A,T)
Reference rs62635655(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 12 not provided
Variation info
Gene CRB1
CLNDBN Retinitis pigmentosa 12 not provided
Reversed 0
HGVS NC_000001.10:g.197403976G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006085.3, RCV000086334.1,