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rs104894916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894916(A;A)
Make rs104894916(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154195934
GeneOPN1MW
is asnp
is mentioned by
dbSNPrs104894916
ebirs104894916
HLIrs104894916
Exacrs104894916
Varsomers104894916
Maprs104894916
PheGenIrs104894916
hapmaprs104894916
1000 genomesrs104894916
hgdprs104894916
ensemblrs104894916
gopubmedrs104894916
geneviewrs104894916
scholarrs104894916
googlers104894916
pharmgkbrs104894916
gwascentralrs104894916
openSNPrs104894916
23andMers104894916
23andMe allrs104894916
SNP Nexus

SNPshotrs104894916
SNPdbers104894916
MSV3drs104894916
GWAS Ctlgrs104894916
Merged fromRs28935199
Max Magnitude0
OMIM300821
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894916(A;A)
Alt rs104894916(A;A)
Reference rs104894916(G;G)
Significance Pathogenic
Disease Colorblindness
Variation info
Gene OPN1MW
CLNDBN Colorblindness, partial, deutan series
Reversed 0
HGVS NC_000023.10:g.153461425G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011255.5,