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

rs794727001

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727001(A;A)
Make rs794727001(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
GenePRPF31
is asnp
is mentioned by
dbSNPrs794727001
ebirs794727001
HLIrs794727001
Exacrs794727001
Varsomers794727001
Maprs794727001
PheGenIrs794727001
hapmaprs794727001
1000 genomesrs794727001
hgdprs794727001
ensemblrs794727001
gopubmedrs794727001
geneviewrs794727001
scholarrs794727001
googlers794727001
pharmgkbrs794727001
gwascentralrs794727001
openSNPrs794727001
23andMers794727001
23andMe allrs794727001
SNP Nexus

SNPshotrs794727001
SNPdbers794727001
MSV3drs794727001
GWAS Ctlgrs794727001
Max Magnitude0
ClinVar
Risk rs794727001(A;A)
Alt rs794727001(A;A)
Reference rs794727001(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 11
Variation info
Gene PRPF31
CLNDBN Retinitis pigmentosa 11
Reversed 0
HGVS NC_000019.9:g.54631576G>A
CLNSRC
CLNACC RCV000173871.1,