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rs786205450

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205450(C;C)
Make rs786205450(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position197421008
GeneCRB1
is asnp
is mentioned by
dbSNPrs786205450
ebirs786205450
HLIrs786205450
Exacrs786205450
Varsomers786205450
Maprs786205450
PheGenIrs786205450
hapmaprs786205450
1000 genomesrs786205450
hgdprs786205450
ensemblrs786205450
gopubmedrs786205450
geneviewrs786205450
scholarrs786205450
googlers786205450
pharmgkbrs786205450
gwascentralrs786205450
openSNPrs786205450
23andMers786205450
23andMe allrs786205450
SNP Nexus

SNPshotrs786205450
SNPdbers786205450
MSV3drs786205450
GWAS Ctlgrs786205450
Max Magnitude0
ClinVar
Risk rs786205450(C;C)
Alt rs786205450(C;C)
Reference rs786205450(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CRB1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.197390138T>C
CLNSRC
CLNACC RCV000171163.1,