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rs267607154

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607154(C;C)
Make rs267607154(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position120788801
GeneTSPAN12
is asnp
is mentioned by
dbSNPrs267607154
ebirs267607154
HLIrs267607154
Exacrs267607154
Varsomers267607154
Maprs267607154
PheGenIrs267607154
hapmaprs267607154
1000 genomesrs267607154
hgdprs267607154
ensemblrs267607154
gopubmedrs267607154
geneviewrs267607154
scholarrs267607154
googlers267607154
pharmgkbrs267607154
gwascentralrs267607154
openSNPrs267607154
23andMers267607154
23andMe allrs267607154
SNP Nexus

SNPshotrs267607154
SNPdbers267607154
MSV3drs267607154
GWAS Ctlgrs267607154
Max Magnitude0
ClinVar
Risk rs267607154(C;C)
Alt rs267607154(C;C)
Reference rs267607154(G;G)
Significance Pathogenic
Disease Exudative vitreoretinopathy 5
Variation info
Gene TSPAN12
CLNDBN Exudative vitreoretinopathy 5
Reversed 1
HGVS NC_000007.13:g.120428855C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000347.3,