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rs121918580

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918580(C;T)
Make rs121918580(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position660590
GenePDE6B
is asnp
is mentioned by
dbSNPrs121918580
ebirs121918580
HLIrs121918580
Exacrs121918580
Varsomers121918580
Maprs121918580
PheGenIrs121918580
hapmaprs121918580
1000 genomesrs121918580
hgdprs121918580
ensemblrs121918580
gopubmedrs121918580
geneviewrs121918580
scholarrs121918580
googlers121918580
pharmgkbrs121918580
gwascentralrs121918580
openSNPrs121918580
23andMers121918580
23andMe allrs121918580
SNP Nexus

SNPshotrs121918580
SNPdbers121918580
MSV3drs121918580
GWAS Ctlgrs121918580
Max Magnitude0
OMIM180072
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918580(G,T;G,T)
Alt rs121918580(G,T;G,T)
Reference rs121918580(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 40
Variation info
Gene PDE6B
CLNDBN Retinitis pigmentosa 40
Reversed 0
HGVS NC_000004.11:g.654379C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013983.27,