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rs267607166

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607166(A;T)
Make rs267607166(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position28552389
GeneUNC119
is asnp
is mentioned by
dbSNPrs267607166
ebirs267607166
HLIrs267607166
Exacrs267607166
Varsomers267607166
Maprs267607166
PheGenIrs267607166
hapmaprs267607166
1000 genomesrs267607166
hgdprs267607166
ensemblrs267607166
gopubmedrs267607166
geneviewrs267607166
scholarrs267607166
googlers267607166
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openSNPrs267607166
23andMers267607166
23andMe allrs267607166
SNP Nexus

SNPshotrs267607166
SNPdbers267607166
MSV3drs267607166
GWAS Ctlgrs267607166
Max Magnitude0
ClinVar
Risk rs267607166(T;T)
Alt rs267607166(T;T)
Reference rs267607166(A;A)
Significance Pathogenic
Disease Cone-rod dystrophy
Variation info
Gene UNC119
CLNDBN Cone-rod dystrophy
Reversed 1
HGVS NC_000017.10:g.26879407T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006240.4,