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rs794727631

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727631(C;T)
Make rs794727631(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position65494921
GeneEYS
is asnp
is mentioned by
dbSNPrs794727631
ebirs794727631
HLIrs794727631
Exacrs794727631
Varsomers794727631
Maprs794727631
PheGenIrs794727631
hapmaprs794727631
1000 genomesrs794727631
hgdprs794727631
ensemblrs794727631
gopubmedrs794727631
geneviewrs794727631
scholarrs794727631
googlers794727631
pharmgkbrs794727631
gwascentralrs794727631
openSNPrs794727631
23andMers794727631
23andMe allrs794727631
SNP Nexus

SNPshotrs794727631
SNPdbers794727631
MSV3drs794727631
GWAS Ctlgrs794727631
Max Magnitude0
ClinVar
Risk rs794727631(T;T)
Alt rs794727631(T;T)
Reference rs794727631(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 25
Variation info
Gene EYS
CLNDBN Retinitis pigmentosa 25
Reversed 1
HGVS NC_000006.11:g.66204814G>A
CLNSRC
CLNACC RCV000178152.1,