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rs878853349

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs878853349(-;-)
Make rs878853349(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position64902132
GeneEYS
is asnp
is mentioned by
dbSNPrs878853349
ebirs878853349
HLIrs878853349
Exacrs878853349
Varsomers878853349
Maprs878853349
PheGenIrs878853349
hapmaprs878853349
1000 genomesrs878853349
hgdprs878853349
ensemblrs878853349
gopubmedrs878853349
geneviewrs878853349
scholarrs878853349
googlers878853349
pharmgkbrs878853349
gwascentralrs878853349
openSNPrs878853349
23andMers878853349
23andMe allrs878853349
SNP Nexus

SNPshotrs878853349
SNPdbers878853349
MSV3drs878853349
GWAS Ctlgrs878853349
Max Magnitude0
ClinVar
Risk rs878853349(;)
Alt rs878853349(;)
Reference rs878853349(AT;AT)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene EYS
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000006.11:g.65612025_65612026delAT
CLNSRC
CLNACC RCV000225412.1,