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rs786200909

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786200909(A;A)
Make rs786200909(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93620620
GenePDE6C
is asnp
is mentioned by
dbSNPrs786200909
ebirs786200909
HLIrs786200909
Exacrs786200909
Varsomers786200909
Maprs786200909
PheGenIrs786200909
hapmaprs786200909
1000 genomesrs786200909
hgdprs786200909
ensemblrs786200909
gopubmedrs786200909
geneviewrs786200909
scholarrs786200909
googlers786200909
pharmgkbrs786200909
gwascentralrs786200909
openSNPrs786200909
23andMers786200909
23andMe allrs786200909
SNP Nexus

SNPshotrs786200909
SNPdbers786200909
MSV3drs786200909
GWAS Ctlgrs786200909
Max Magnitude0
ClinVar
Risk rs786200909(A;A)
Alt rs786200909(A;A)
Reference rs786200909(T;T)
Significance Pathogenic
Disease Achromatopsia 5
Variation info
Gene PDE6C
CLNDBN Achromatopsia 5
Reversed 0
HGVS NC_000010.10:g.95380377T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009315.4,