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rs527236115

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236115(A;A)
Make rs527236115(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position96293481
GeneSNRNP200
is asnp
is mentioned by
dbSNPrs527236115
ebirs527236115
HLIrs527236115
Exacrs527236115
Varsomers527236115
Maprs527236115
PheGenIrs527236115
hapmaprs527236115
1000 genomesrs527236115
hgdprs527236115
ensemblrs527236115
gopubmedrs527236115
geneviewrs527236115
scholarrs527236115
googlers527236115
pharmgkbrs527236115
gwascentralrs527236115
openSNPrs527236115
23andMers527236115
23andMe allrs527236115
SNP Nexus

SNPshotrs527236115
SNPdbers527236115
MSV3drs527236115
GWAS Ctlgrs527236115
Max Magnitude0
ClinVar
Risk rs527236115(A;A)
Alt rs527236115(A;A)
Reference rs527236115(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa Retinal dystrophy
Variation info
Gene SNRNP200
CLNDBN Retinitis pigmentosa Retinal dystrophy
Reversed 1
HGVS NC_000002.11:g.96959219C>T
CLNSRC ClinVar
CLNACC RCV000132668.1, RCV000225495.1,