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rs527236113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236113(A;A)
Make rs527236113(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position96293090
GeneSNRNP200
is asnp
is mentioned by
dbSNPrs527236113
ebirs527236113
HLIrs527236113
Exacrs527236113
Varsomers527236113
Maprs527236113
PheGenIrs527236113
hapmaprs527236113
1000 genomesrs527236113
hgdprs527236113
ensemblrs527236113
gopubmedrs527236113
geneviewrs527236113
scholarrs527236113
googlers527236113
pharmgkbrs527236113
gwascentralrs527236113
openSNPrs527236113
23andMers527236113
23andMe allrs527236113
SNP Nexus

SNPshotrs527236113
SNPdbers527236113
MSV3drs527236113
GWAS Ctlgrs527236113
Max Magnitude0
ClinVar
Risk rs527236113(A;A)
Alt rs527236113(A;A)
Reference rs527236113(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene SNRNP200
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000002.11:g.96958828C>T
CLNSRC ClinVar
CLNACC RCV000132669.1,