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rs137853189

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853189(G;T)
Make rs137853189(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position64436244
GeneEYS
is asnp
is mentioned by
dbSNPrs137853189
ebirs137853189
HLIrs137853189
Exacrs137853189
Varsomers137853189
Maprs137853189
PheGenIrs137853189
hapmaprs137853189
1000 genomesrs137853189
hgdprs137853189
ensemblrs137853189
gopubmedrs137853189
geneviewrs137853189
scholarrs137853189
googlers137853189
pharmgkbrs137853189
gwascentralrs137853189
openSNPrs137853189
23andMers137853189
23andMe allrs137853189
SNP Nexus

SNPshotrs137853189
SNPdbers137853189
MSV3drs137853189
GWAS Ctlgrs137853189
Max Magnitude0
OMIM612424
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853189(T;T)
Alt rs137853189(T;T)
Reference rs137853189(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 25
Variation info
Gene EYS
CLNDBN Retinitis pigmentosa 25
Reversed 1
HGVS NC_000006.11:g.65146137C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000567.3,