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rs62636267

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs62636267(C;C)
Make rs62636267(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position197427547
GeneCRB1
is asnp
is mentioned by
dbSNPrs62636267
dbSNP (classic)rs62636267
ClinGenrs62636267
ebirs62636267
HLIrs62636267
Exacrs62636267
Gnomadrs62636267
Varsomers62636267
LitVarrs62636267
Maprs62636267
PheGenIrs62636267
Biobankrs62636267
1000 genomesrs62636267
hgdprs62636267
ensemblrs62636267
geneviewrs62636267
scholarrs62636267
googlers62636267
pharmgkbrs62636267
gwascentralrs62636267
openSNPrs62636267
23andMers62636267
23andMe allrs62636267
SNPshotrs62636267
SNPdbers62636267
MSV3drs62636267
GWAS Ctlgrs62636267
Max Magnitude0
ClinVar
Risk rs62636267(C;C)
Alt rs62636267(C;C)
Reference Rs62636267(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CRB1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.197396677T>C
CLNSRC UniProtKB (protein)
CLNACC RCV000086314.2,