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rs121918583

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918583(A;A)
Make rs121918583(A;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position667922
GenePDE6B
is asnp
is mentioned by
dbSNPrs121918583
ebirs121918583
HLIrs121918583
Exacrs121918583
Varsomers121918583
Maprs121918583
PheGenIrs121918583
hapmaprs121918583
1000 genomesrs121918583
hgdprs121918583
ensemblrs121918583
gopubmedrs121918583
geneviewrs121918583
scholarrs121918583
googlers121918583
pharmgkbrs121918583
gwascentralrs121918583
openSNPrs121918583
23andMers121918583
23andMe allrs121918583
SNP Nexus

SNPshotrs121918583
SNPdbers121918583
MSV3drs121918583
GWAS Ctlgrs121918583
Max Magnitude0
OMIM180072
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918583(A,C;A,C)
Alt rs121918583(A,C;A,C)
Reference rs121918583(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 40
Variation info
Gene PDE6B
CLNDBN Retinitis pigmentosa 40
Reversed 0
HGVS NC_000004.11:g.661711T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013988.26,