Have questions? Visit https://www.reddit.com/r/SNPedia

rs797045089

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045089(A;A)
Make rs797045089(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position64081899
GeneEYS
is asnp
is mentioned by
dbSNPrs797045089
ebirs797045089
HLIrs797045089
Exacrs797045089
Varsomers797045089
Maprs797045089
PheGenIrs797045089
hapmaprs797045089
1000 genomesrs797045089
hgdprs797045089
ensemblrs797045089
gopubmedrs797045089
geneviewrs797045089
scholarrs797045089
googlers797045089
pharmgkbrs797045089
gwascentralrs797045089
openSNPrs797045089
23andMers797045089
23andMe allrs797045089
SNP Nexus

SNPshotrs797045089
SNPdbers797045089
MSV3drs797045089
GWAS Ctlgrs797045089
Max Magnitude0
ClinVar
Risk rs797045089(A;A)
Alt rs797045089(A;A)
Reference rs797045089(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 25
Variation info
Gene EYS
CLNDBN Retinitis pigmentosa 25
Reversed 1
HGVS NC_000006.11:g.64791792G>T
CLNSRC
CLNACC RCV000190583.1,