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rs387906401

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906401(C;C)
Make rs387906401(C;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position93620784
GenePDE6C
is asnp
is mentioned by
dbSNPrs387906401
ebirs387906401
HLIrs387906401
Exacrs387906401
Varsomers387906401
Maprs387906401
PheGenIrs387906401
hapmaprs387906401
1000 genomesrs387906401
hgdprs387906401
ensemblrs387906401
gopubmedrs387906401
geneviewrs387906401
scholarrs387906401
googlers387906401
pharmgkbrs387906401
gwascentralrs387906401
openSNPrs387906401
23andMers387906401
23andMe allrs387906401
SNP Nexus

SNPshotrs387906401
SNPdbers387906401
MSV3drs387906401
GWAS Ctlgrs387906401
Max Magnitude0
ClinVar
Risk rs387906401(C;C)
Alt rs387906401(C;C)
Reference rs387906401(G;G)
Significance Pathogenic
Disease Achromatopsia 5
Variation info
Gene PDE6C
CLNDBN Achromatopsia 5
Reversed 0
HGVS NC_000010.10:g.95380541G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009313.4,