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rs62635656

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs62635656(C;C)
Make rs62635656(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position197434985
GeneCRB1
is asnp
is mentioned by
dbSNPrs62635656
dbSNP (old)rs62635656
ClinGenrs62635656
ebirs62635656
HLIrs62635656
Exacrs62635656
Varsomers62635656
Maprs62635656
PheGenIrs62635656
Biobankrs62635656
1000 genomesrs62635656
hgdprs62635656
ensemblrs62635656
gopubmedrs62635656
geneviewrs62635656
scholarrs62635656
googlers62635656
pharmgkbrs62635656
gwascentralrs62635656
openSNPrs62635656
23andMers62635656
23andMe allrs62635656
SNP Nexus

SNPshotrs62635656
SNPdbers62635656
MSV3drs62635656
GWAS Ctlgrs62635656
Max Magnitude0
OMIM604210
Desc
Variant0002
Relatedalso


ClinVar
Risk rs62635656(C;C)
Alt rs62635656(C;C)
Reference Rs62635656(T;T)
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.197404115T>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000006084.3, RCV000086336.1,