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rs104894912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894912(C;T)
Make rs104894912(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154154734
GeneOPN1LW
is asnp
is mentioned by
dbSNPrs104894912
ebirs104894912
HLIrs104894912
Exacrs104894912
Varsomers104894912
Maprs104894912
PheGenIrs104894912
hapmaprs104894912
1000 genomesrs104894912
hgdprs104894912
ensemblrs104894912
gopubmedrs104894912
geneviewrs104894912
scholarrs104894912
googlers104894912
pharmgkbrs104894912
gwascentralrs104894912
openSNPrs104894912
23andMers104894912
23andMe allrs104894912
SNP Nexus

SNPshotrs104894912
SNPdbers104894912
MSV3drs104894912
GWAS Ctlgrs104894912
Max Magnitude0
ClinVar
Risk rs104894912(T;T)
Alt rs104894912(T;T)
Reference rs104894912(C;C)
Significance Pathogenic
Disease Cone monochromatism
Variation info
Gene OPN1LW
CLNDBN Cone monochromatism
Reversed 0
HGVS NC_000023.10:g.153420209C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011249.7,