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rs104894913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894913(A;A)
Make rs104894913(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154158844
GeneOPN1LW
is asnp
is mentioned by
dbSNPrs104894913
ebirs104894913
HLIrs104894913
Exacrs104894913
Varsomers104894913
Maprs104894913
PheGenIrs104894913
hapmaprs104894913
1000 genomesrs104894913
hgdprs104894913
ensemblrs104894913
gopubmedrs104894913
geneviewrs104894913
scholarrs104894913
googlers104894913
pharmgkbrs104894913
gwascentralrs104894913
openSNPrs104894913
23andMers104894913
23andMe allrs104894913
SNP Nexus

SNPshotrs104894913
SNPdbers104894913
MSV3drs104894913
GWAS Ctlgrs104894913
Max Magnitude0
ClinVar
Risk rs104894913(A;A)
Alt rs104894913(A;A)
Reference rs104894913(G;G)
Significance Pathogenic
Disease Protan defect
Variation info
Gene OPN1LW
CLNDBN Protan defect
Reversed 0
HGVS NC_000023.10:g.153424319G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011252.3,