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rs863224863

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224863(A;A)
Make rs863224863(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position47836266
GeneCRX
is asnp
is mentioned by
dbSNPrs863224863
ebirs863224863
HLIrs863224863
Exacrs863224863
Varsomers863224863
Maprs863224863
PheGenIrs863224863
hapmaprs863224863
1000 genomesrs863224863
hgdprs863224863
ensemblrs863224863
gopubmedrs863224863
geneviewrs863224863
scholarrs863224863
googlers863224863
pharmgkbrs863224863
gwascentralrs863224863
openSNPrs863224863
23andMers863224863
23andMe allrs863224863
SNP Nexus

SNPshotrs863224863
SNPdbers863224863
MSV3drs863224863
GWAS Ctlgrs863224863
Max Magnitude0
ClinVar
Risk rs863224863(A;A)
Alt rs863224863(A;A)
Reference rs863224863(G;G)
Significance Probable-Pathogenic
Disease Leber congenital amaurosis 7
Variation info
Gene CRX
CLNDBN Leber congenital amaurosis 7
Reversed 0
HGVS NC_000019.9:g.48339523G>A
CLNSRC
CLNACC RCV000197997.1,