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rs267607077

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607077(C;T)
Make rs267607077(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position96287968
GeneSNRNP200
is asnp
is mentioned by
dbSNPrs267607077
ebirs267607077
HLIrs267607077
Exacrs267607077
Varsomers267607077
Maprs267607077
PheGenIrs267607077
hapmaprs267607077
1000 genomesrs267607077
hgdprs267607077
ensemblrs267607077
gopubmedrs267607077
geneviewrs267607077
scholarrs267607077
googlers267607077
pharmgkbrs267607077
gwascentralrs267607077
openSNPrs267607077
23andMers267607077
23andMe allrs267607077
SNP Nexus

SNPshotrs267607077
SNPdbers267607077
MSV3drs267607077
GWAS Ctlgrs267607077
Max Magnitude0
ClinVar
Risk rs267607077(T;T)
Alt rs267607077(T;T)
Reference rs267607077(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 33
Variation info
Gene SNRNP200
CLNDBN Retinitis pigmentosa 33
Reversed 1
HGVS NC_000002.11:g.96953706G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008390.3,