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rs397509379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509379(C;G)
Make rs397509379(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position109869900
GeneLRIT3
is asnp
is mentioned by
dbSNPrs397509379
ebirs397509379
HLIrs397509379
Exacrs397509379
Varsomers397509379
Maprs397509379
PheGenIrs397509379
hapmaprs397509379
1000 genomesrs397509379
hgdprs397509379
ensemblrs397509379
gopubmedrs397509379
geneviewrs397509379
scholarrs397509379
googlers397509379
pharmgkbrs397509379
gwascentralrs397509379
openSNPrs397509379
23andMers397509379
23andMe allrs397509379
SNP Nexus

SNPshotrs397509379
SNPdbers397509379
MSV3drs397509379
GWAS Ctlgrs397509379
Max Magnitude0
ClinVar
Risk rs397509379(G;G)
Alt rs397509379(G;G)
Reference rs397509379(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.110791056C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000032635.3,