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rs61748449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61748449(-;-)
Make rs61748449(-;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position47839596
GeneCRX
is asnp
is mentioned by
dbSNPrs61748449
ebirs61748449
HLIrs61748449
Exacrs61748449
Varsomers61748449
Maprs61748449
PheGenIrs61748449
hapmaprs61748449
1000 genomesrs61748449
hgdprs61748449
ensemblrs61748449
gopubmedrs61748449
geneviewrs61748449
scholarrs61748449
googlers61748449
pharmgkbrs61748449
gwascentralrs61748449
openSNPrs61748449
23andMers61748449
23andMe allrs61748449
SNP Nexus

SNPshotrs61748449
SNPdbers61748449
MSV3drs61748449
GWAS Ctlgrs61748449
Max Magnitude0
ClinVar
Risk rs61748449(;)
Alt rs61748449(;)
Reference rs61748449(G;G)
Significance Pathogenic
Disease Leber congenital amaurosis 7 not provided
Variation info
Gene CRX
CLNDBN Leber congenital amaurosis 7 not provided
Reversed 0
HGVS NC_000019.9:g.48342853delG
CLNSRC ClinVar GeneReviews Retina International
CLNACC RCV000055824.1, RCV000086008.1,