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rs786200908

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs786200908(-;AG)
Make rs786200908(AG;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93612982
GenePDE6C
is asnp
is mentioned by
dbSNPrs786200908
ClinGenrs786200908
ebirs786200908
HLIrs786200908
Exacrs786200908
Varsomers786200908
Maprs786200908
PheGenIrs786200908
hapmaprs786200908
1000 genomesrs786200908
hgdprs786200908
ensemblrs786200908
gopubmedrs786200908
geneviewrs786200908
scholarrs786200908
googlers786200908
pharmgkbrs786200908
gwascentralrs786200908
openSNPrs786200908
23andMers786200908
23andMe allrs786200908
SNP Nexus

SNPshotrs786200908
SNPdbers786200908
MSV3drs786200908
GWAS Ctlgrs786200908
Max Magnitude0
ClinVar
Risk rs786200908(AG;AG)
Alt rs786200908(AG;AG)
Reference Rs786200908(;)
Significance Pathogenic
Disease Achromatopsia 5
Variation info
Gene PDE6C
CLNDBN Achromatopsia 5
Reversed 0
HGVS NC_000010.10:g.95372738_95372739dupAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000009310.4,