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rs786200911

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786200911(-;-)
Make rs786200911(-;A)
Make rs786200911(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93640502
GenePDE6C
is asnp
is mentioned by
dbSNPrs786200911
ebirs786200911
HLIrs786200911
Exacrs786200911
Varsomers786200911
Maprs786200911
PheGenIrs786200911
hapmaprs786200911
1000 genomesrs786200911
hgdprs786200911
ensemblrs786200911
gopubmedrs786200911
geneviewrs786200911
scholarrs786200911
googlers786200911
pharmgkbrs786200911
gwascentralrs786200911
openSNPrs786200911
23andMers786200911
23andMe allrs786200911
SNP Nexus

SNPshotrs786200911
SNPdbers786200911
MSV3drs786200911
GWAS Ctlgrs786200911
Max Magnitude0
ClinVar
Risk rs786200911(A;A)
Alt rs786200911(A;A)
Reference rs786200911(;)
Significance Pathogenic
Disease Achromatopsia 5
Variation info
Gene PDE6C
CLNDBN Achromatopsia 5
Reversed 0
HGVS NC_000010.10:g.95400259dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000009320.4,