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rs786205852

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205852(-;-)
Make rs786205852(-;A)
Make rs786205852(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67455504
GeneCABP4
is asnp
is mentioned by
dbSNPrs786205852
ebirs786205852
HLIrs786205852
Exacrs786205852
Varsomers786205852
Maprs786205852
PheGenIrs786205852
hapmaprs786205852
1000 genomesrs786205852
hgdprs786205852
ensemblrs786205852
gopubmedrs786205852
geneviewrs786205852
scholarrs786205852
googlers786205852
pharmgkbrs786205852
gwascentralrs786205852
openSNPrs786205852
23andMers786205852
23andMe allrs786205852
SNP Nexus

SNPshotrs786205852
SNPdbers786205852
MSV3drs786205852
GWAS Ctlgrs786205852
Max Magnitude0
ClinVar
Risk rs786205852(A;A)
Alt rs786205852(A;A)
Reference rs786205852(;)
Significance Pathogenic
Disease Congenital stationary night blindness
Variation info
Gene CABP4
CLNDBN Congenital stationary night blindness, type 2B
Reversed 0
HGVS NC_000011.9:g.67222975_67222976insA
CLNSRC OMIM Allelic Variant
CLNACC RCV000171133.2,