Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223340

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223340(G;G)
Make rs863223340(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position54622180
GeneRP1
is asnp
is mentioned by
dbSNPrs863223340
dbSNP (classic)rs863223340
ClinGenrs863223340
ebirs863223340
HLIrs863223340
Exacrs863223340
Gnomadrs863223340
Varsomers863223340
LitVarrs863223340
Maprs863223340
PheGenIrs863223340
Biobankrs863223340
1000 genomesrs863223340
hgdprs863223340
ensemblrs863223340
geneviewrs863223340
scholarrs863223340
googlers863223340
pharmgkbrs863223340
gwascentralrs863223340
openSNPrs863223340
23andMers863223340
SNPshotrs863223340
SNPdbers863223340
MSV3drs863223340
GWAS Ctlgrs863223340
Max Magnitude0
ClinVar
Risk rs863223340(G;G)
Alt rs863223340(G;G)
Reference Rs863223340(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RP1
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000008.10:g.55534740T>G
CLNSRC
CLNACC RCV000201456.1,