Have questions? Visit https://www.reddit.com/r/SNPedia

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
dbSNP (classic)rs267607166
ClinGenrs267607166
ebirs267607166
HLIrs267607166
Exacrs267607166
Gnomadrs267607166
Varsomers267607166
LitVarrs267607166
Maprs267607166
PheGenIrs267607166
Biobankrs267607166
1000 genomesrs267607166
hgdprs267607166
ensemblrs267607166
geneviewrs267607166
scholarrs267607166
googlers267607166
pharmgkbrs267607166
gwascentralrs267607166
openSNPrs267607166
23andMers267607166
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,