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rs878853350

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853350(A;A)
Make rs878853350(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position64307024
GeneEYS
is asnp
is mentioned by
dbSNPrs878853350
ebirs878853350
HLIrs878853350
Exacrs878853350
Varsomers878853350
Maprs878853350
PheGenIrs878853350
hapmaprs878853350
1000 genomesrs878853350
hgdprs878853350
ensemblrs878853350
gopubmedrs878853350
geneviewrs878853350
scholarrs878853350
googlers878853350
pharmgkbrs878853350
gwascentralrs878853350
openSNPrs878853350
23andMers878853350
23andMe allrs878853350
SNP Nexus

SNPshotrs878853350
SNPdbers878853350
MSV3drs878853350
GWAS Ctlgrs878853350
Max Magnitude0
ClinVar
Risk rs878853350(A;A)
Alt rs878853350(A;A)
Reference rs878853350(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene EYS
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000006.11:g.65016917C>T
CLNSRC
CLNACC RCV000225657.1,