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rs376610215

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376610215(A;A)
Make rs376610215(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position109869732
GeneLRIT3
is asnp
is mentioned by
dbSNPrs376610215
ebirs376610215
HLIrs376610215
Exacrs376610215
Varsomers376610215
Maprs376610215
PheGenIrs376610215
hapmaprs376610215
1000 genomesrs376610215
hgdprs376610215
ensemblrs376610215
gopubmedrs376610215
geneviewrs376610215
scholarrs376610215
googlers376610215
pharmgkbrs376610215
gwascentralrs376610215
openSNPrs376610215
23andMers376610215
23andMe allrs376610215
SNP Nexus

SNPshotrs376610215
SNPdbers376610215
MSV3drs376610215
GWAS Ctlgrs376610215
Max Magnitude0
ClinVar
Risk rs376610215(A;A)
Alt rs376610215(A;A)
Reference rs376610215(G;G)
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.110790888G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032633.2,