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rs137853291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853291(A;A)
Make rs137853291(A;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position89211750
GeneRLBP1
is asnp
is mentioned by
dbSNPrs137853291
ebirs137853291
HLIrs137853291
Exacrs137853291
Varsomers137853291
Maprs137853291
PheGenIrs137853291
hapmaprs137853291
1000 genomesrs137853291
hgdprs137853291
ensemblrs137853291
gopubmedrs137853291
geneviewrs137853291
scholarrs137853291
googlers137853291
pharmgkbrs137853291
gwascentralrs137853291
openSNPrs137853291
23andMers137853291
23andMe allrs137853291
SNP Nexus

SNPshotrs137853291
SNPdbers137853291
MSV3drs137853291
GWAS Ctlgrs137853291
Max Magnitude0
OMIM180090
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853291(A;A)
Alt rs137853291(A;A)
Reference rs137853291(T;T)
Significance Pathogenic
Disease Retinitis punctata albescens
Variation info
Gene RLBP1
CLNDBN Retinitis punctata albescens
Reversed 1
HGVS NC_000015.9:g.89754981A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013980.24,