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rs724159983

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs724159983(A;C)
Make rs724159983(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154182566
GeneOPN1MW
is asnp
is mentioned by
dbSNPrs724159983
ebirs724159983
HLIrs724159983
Exacrs724159983
Varsomers724159983
Maprs724159983
PheGenIrs724159983
hapmaprs724159983
1000 genomesrs724159983
hgdprs724159983
ensemblrs724159983
gopubmedrs724159983
geneviewrs724159983
scholarrs724159983
googlers724159983
pharmgkbrs724159983
gwascentralrs724159983
openSNPrs724159983
23andMers724159983
23andMe allrs724159983
SNP Nexus

SNPshotrs724159983
SNPdbers724159983
MSV3drs724159983
GWAS Ctlgrs724159983
Max Magnitude0
ClinVar
Risk rs724159983(C;C)
Alt rs724159983(C;C)
Reference rs724159983(A;A)
Significance Pathogenic
Disease Colorblindness
Variation info
Gene OPN1MW
CLNDBN Colorblindness, partial, deutan series
Reversed 0
HGVS NC_000023.10:g.153448055A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011256.3,