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rs782215106

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs782215106(A;A)
Make rs782215106(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position47348733
GeneRBP3
is asnp
is mentioned by
dbSNPrs782215106
ebirs782215106
HLIrs782215106
Exacrs782215106
Varsomers782215106
Maprs782215106
PheGenIrs782215106
hapmaprs782215106
1000 genomesrs782215106
hgdprs782215106
ensemblrs782215106
gopubmedrs782215106
geneviewrs782215106
scholarrs782215106
googlers782215106
pharmgkbrs782215106
gwascentralrs782215106
openSNPrs782215106
23andMers782215106
23andMe allrs782215106
SNP Nexus

SNPshotrs782215106
SNPdbers782215106
MSV3drs782215106
GWAS Ctlgrs782215106
Max Magnitude0
ClinVar
Risk rs782215106(A,T;A,T)
Alt rs782215106(A,T;A,T)
Reference rs782215106(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RBP3
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000010.10:g.48390629G>T
CLNSRC
CLNACC RCV000210317.1,