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rs1060499783

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499783(C;T)
Make rs1060499783(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position63984462
GeneEYS, LOC107986608
is asnp
is mentioned by
dbSNPrs1060499783
dbSNP (old)rs1060499783
ClinGenrs1060499783
ebirs1060499783
HLIrs1060499783
Exacrs1060499783
Gnomadrs1060499783
Varsomers1060499783
Maprs1060499783
PheGenIrs1060499783
Biobankrs1060499783
1000 genomesrs1060499783
hgdprs1060499783
ensemblrs1060499783
gopubmedrs1060499783
geneviewrs1060499783
scholarrs1060499783
googlers1060499783
pharmgkbrs1060499783
gwascentralrs1060499783
openSNPrs1060499783
23andMers1060499783
23andMe allrs1060499783
SNPshotrs1060499783
SNPdbers1060499783
MSV3drs1060499783
GWAS Ctlgrs1060499783
Max Magnitude0
ClinVar
Risk rs1060499783(T;T)
Alt rs1060499783(T;T)
Reference Rs1060499783(C;C)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa 25
Variation info
Gene EYS
CLNDBN Retinitis pigmentosa 25
Reversed 1
HGVS NC_000006.11:g.64694355G>A
CLNSRC
CLNACC RCV000454133.1,