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rs267607151

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607151(C;C)
Make rs267607151(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position120806599
GeneTSPAN12
is asnp
is mentioned by
dbSNPrs267607151
ebirs267607151
HLIrs267607151
Exacrs267607151
Varsomers267607151
Maprs267607151
PheGenIrs267607151
hapmaprs267607151
1000 genomesrs267607151
hgdprs267607151
ensemblrs267607151
gopubmedrs267607151
geneviewrs267607151
scholarrs267607151
googlers267607151
pharmgkbrs267607151
gwascentralrs267607151
openSNPrs267607151
23andMers267607151
23andMe allrs267607151
SNP Nexus

SNPshotrs267607151
SNPdbers267607151
MSV3drs267607151
GWAS Ctlgrs267607151
Max Magnitude0
ClinVar
Risk rs267607151(C;C)
Alt rs267607151(C;C)
Reference rs267607151(G;G)
Significance Pathogenic
Disease Exudative vitreoretinopathy 5
Variation info
Gene TSPAN12
CLNDBN Exudative vitreoretinopathy 5
Reversed 1
HGVS NC_000007.13:g.120446653C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000348.3,