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rs397509380

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397509380(-;-)
Make rs397509380(-;CT)
ReferenceGRCh38 38.1/141
Chromosome4
Position109870287
GeneLRIT3
is asnp
is mentioned by
dbSNPrs397509380
ebirs397509380
HLIrs397509380
Exacrs397509380
Varsomers397509380
Maprs397509380
PheGenIrs397509380
hapmaprs397509380
1000 genomesrs397509380
hgdprs397509380
ensemblrs397509380
gopubmedrs397509380
geneviewrs397509380
scholarrs397509380
googlers397509380
pharmgkbrs397509380
gwascentralrs397509380
openSNPrs397509380
23andMers397509380
23andMe allrs397509380
SNP Nexus

SNPshotrs397509380
SNPdbers397509380
MSV3drs397509380
GWAS Ctlgrs397509380
Max Magnitude0
ClinVar
Risk rs397509380(;)
Alt rs397509380(;)
Reference rs397509380(CT;CT)
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.110791443_110791444delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000032636.3,