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rs121434621

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434621(C;C)
Make rs121434621(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154154602
GeneOPN1LW
is asnp
is mentioned by
dbSNPrs121434621
ebirs121434621
HLIrs121434621
Exacrs121434621
Varsomers121434621
Maprs121434621
PheGenIrs121434621
hapmaprs121434621
1000 genomesrs121434621
hgdprs121434621
ensemblrs121434621
gopubmedrs121434621
geneviewrs121434621
scholarrs121434621
googlers121434621
pharmgkbrs121434621
gwascentralrs121434621
openSNPrs121434621
23andMers121434621
23andMe allrs121434621
SNP Nexus

SNPshotrs121434621
SNPdbers121434621
MSV3drs121434621
GWAS Ctlgrs121434621
Max Magnitude0
ClinVar
Risk rs121434621(C;C)
Alt rs121434621(C;C)
Reference rs121434621(T;T)
Significance Pathogenic
Disease Cone monochromatism
Variation info
Gene OPN1LW
CLNDBN Cone monochromatism
Reversed 0
HGVS NC_000023.10:g.153420077T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011251.6,