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rs758052437

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758052437(C;C)
Make rs758052437(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position663143
GeneLOC102725200, PDE6B
is asnp
is mentioned by
dbSNPrs758052437
ebirs758052437
HLIrs758052437
Exacrs758052437
Varsomers758052437
Maprs758052437
PheGenIrs758052437
hapmaprs758052437
1000 genomesrs758052437
hgdprs758052437
ensemblrs758052437
gopubmedrs758052437
geneviewrs758052437
scholarrs758052437
googlers758052437
pharmgkbrs758052437
gwascentralrs758052437
openSNPrs758052437
23andMers758052437
23andMe allrs758052437
SNP Nexus

SNPshotrs758052437
SNPdbers758052437
MSV3drs758052437
GWAS Ctlgrs758052437
Max Magnitude0
ClinVar
Risk rs758052437(C;C)
Alt rs758052437(C;C)
Reference rs758052437(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa 40
Variation info
Gene PDE6B LOC101928494
CLNDBN Retinitis pigmentosa 40
Reversed 0
HGVS NC_000004.11:g.656932G>T
CLNSRC
CLNACC RCV000210313.1,