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

rs730880317

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880317(-;-)
Make rs730880317(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position660487
GenePDE6B
is asnp
is mentioned by
dbSNPrs730880317
ebirs730880317
HLIrs730880317
Exacrs730880317
Varsomers730880317
Maprs730880317
PheGenIrs730880317
hapmaprs730880317
1000 genomesrs730880317
hgdprs730880317
ensemblrs730880317
gopubmedrs730880317
geneviewrs730880317
scholarrs730880317
googlers730880317
pharmgkbrs730880317
gwascentralrs730880317
openSNPrs730880317
23andMers730880317
23andMe allrs730880317
SNP Nexus

SNPshotrs730880317
SNPdbers730880317
MSV3drs730880317
GWAS Ctlgrs730880317
Max Magnitude0
ClinVar
Risk rs730880317(;)
Alt rs730880317(;)
Reference rs730880317(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 40
Variation info
Gene PDE6B
CLNDBN Retinitis pigmentosa 40
Reversed 0
HGVS NC_000004.11:g.654276delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000013984.25,