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rs863223339

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223339(G;T)
Make rs863223339(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position656244
GeneLOC101928521, PDE6B
is asnp
is mentioned by
dbSNPrs863223339
ebirs863223339
HLIrs863223339
Exacrs863223339
Varsomers863223339
Maprs863223339
PheGenIrs863223339
hapmaprs863223339
1000 genomesrs863223339
hgdprs863223339
ensemblrs863223339
gopubmedrs863223339
geneviewrs863223339
scholarrs863223339
googlers863223339
pharmgkbrs863223339
gwascentralrs863223339
openSNPrs863223339
23andMers863223339
23andMe allrs863223339
SNP Nexus

SNPshotrs863223339
SNPdbers863223339
MSV3drs863223339
GWAS Ctlgrs863223339
Max Magnitude0
ClinVar
Risk rs863223339(T;T)
Alt rs863223339(T;T)
Reference rs863223339(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PDE6B RP11-1191J2.2
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000004.11:g.650033G>T
CLNSRC
CLNACC RCV000201503.1,