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rs794727120

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727120(C;T)
Make rs794727120(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position64997647
GeneEYS
is asnp
is mentioned by
dbSNPrs794727120
ebirs794727120
HLIrs794727120
Exacrs794727120
Varsomers794727120
Maprs794727120
PheGenIrs794727120
hapmaprs794727120
1000 genomesrs794727120
hgdprs794727120
ensemblrs794727120
gopubmedrs794727120
geneviewrs794727120
scholarrs794727120
googlers794727120
pharmgkbrs794727120
gwascentralrs794727120
openSNPrs794727120
23andMers794727120
23andMe allrs794727120
SNP Nexus

SNPshotrs794727120
SNPdbers794727120
MSV3drs794727120
GWAS Ctlgrs794727120
Max Magnitude0
ClinVar
Risk rs794727120(T;T)
Alt rs794727120(T;T)
Reference rs794727120(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 25
Variation info
Gene EYS
CLNDBN Retinitis pigmentosa 25
Reversed 1
HGVS NC_000006.11:g.65707540G>A
CLNSRC
CLNACC RCV000174711.1,