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rs878853383

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853383(-;-)
Make rs878853383(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position47839672
GeneCRX
is asnp
is mentioned by
dbSNPrs878853383
ebirs878853383
HLIrs878853383
Exacrs878853383
Varsomers878853383
Maprs878853383
PheGenIrs878853383
hapmaprs878853383
1000 genomesrs878853383
hgdprs878853383
ensemblrs878853383
gopubmedrs878853383
geneviewrs878853383
scholarrs878853383
googlers878853383
pharmgkbrs878853383
gwascentralrs878853383
openSNPrs878853383
23andMers878853383
23andMe allrs878853383
SNP Nexus

SNPshotrs878853383
SNPdbers878853383
MSV3drs878853383
GWAS Ctlgrs878853383
Max Magnitude0
ClinVar
Risk rs878853383(;)
Alt rs878853383(;)
Reference rs878853383(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CRX
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000019.9:g.48342929delG
CLNSRC
CLNACC RCV000225573.1,