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rs398123576

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123576(-;-)
Make rs398123576(-;A)
Make rs398123576(A;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position63721622
GeneEYS
is asnp
is mentioned by
dbSNPrs398123576
ebirs398123576
HLIrs398123576
Exacrs398123576
Varsomers398123576
Maprs398123576
PheGenIrs398123576
hapmaprs398123576
1000 genomesrs398123576
hgdprs398123576
ensemblrs398123576
gopubmedrs398123576
geneviewrs398123576
scholarrs398123576
googlers398123576
pharmgkbrs398123576
gwascentralrs398123576
openSNPrs398123576
23andMers398123576
23andMe allrs398123576
SNP Nexus

SNPshotrs398123576
SNPdbers398123576
MSV3drs398123576
GWAS Ctlgrs398123576
Max Magnitude0
ClinVar
Risk rs398123576(A;A)
Alt rs398123576(A;A)
Reference rs398123576(;)
Significance Pathogenic
Disease not provided Retinitis pigmentosa 25
Variation info
Gene EYS
CLNDBN not provided Retinitis pigmentosa 25
Reversed 1
HGVS NC_000006.11:g.64431519dupT
CLNSRC ClinVar
CLNACC RCV000079547.3, RCV000178517.1,