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rs527236069

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236069(-;-)
Make rs527236069(-;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position63984390
GeneEYS, LOC107986608
is asnp
is mentioned by
dbSNPrs527236069
dbSNP (classic)rs527236069
ClinGenrs527236069
ebirs527236069
HLIrs527236069
Exacrs527236069
Gnomadrs527236069
Varsomers527236069
LitVarrs527236069
Maprs527236069
PheGenIrs527236069
Biobankrs527236069
1000 genomesrs527236069
hgdprs527236069
ensemblrs527236069
geneviewrs527236069
scholarrs527236069
googlers527236069
pharmgkbrs527236069
gwascentralrs527236069
openSNPrs527236069
23andMers527236069
SNPshotrs527236069
SNPdbers527236069
MSV3drs527236069
GWAS Ctlgrs527236069
Max Magnitude0
ClinVar
Risk rs527236069(-;-)
Alt rs527236069(-;-)
Reference Rs527236069(T;T)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene EYS
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000006.11:g.64694283delA
CLNSRC ClinVar
CLNACC RCV000132630.1,