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rs397509378

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509378(C;T)
Make rs397509378(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position109870067
GeneLRIT3
is asnp
is mentioned by
dbSNPrs397509378
ebirs397509378
HLIrs397509378
Exacrs397509378
Varsomers397509378
Maprs397509378
PheGenIrs397509378
hapmaprs397509378
1000 genomesrs397509378
hgdprs397509378
ensemblrs397509378
gopubmedrs397509378
geneviewrs397509378
scholarrs397509378
googlers397509378
pharmgkbrs397509378
gwascentralrs397509378
openSNPrs397509378
23andMers397509378
23andMe allrs397509378
SNP Nexus

SNPshotrs397509378
SNPdbers397509378
MSV3drs397509378
GWAS Ctlgrs397509378
Max Magnitude0
ClinVar
Risk rs397509378(T;T)
Alt rs397509378(T;T)
Reference rs397509378(C;C)
Significance Pathogenic
Disease Congenital stationary night blindness
Variation info
Gene LRIT3
CLNDBN Congenital stationary night blindness, type 1F
Reversed 0
HGVS NC_000004.11:g.110791223C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032634.2,