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rs267607152

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607152(A;A)
Make rs267607152(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position120815787
GeneTSPAN12
is asnp
is mentioned by
dbSNPrs267607152
ebirs267607152
HLIrs267607152
Exacrs267607152
Varsomers267607152
Maprs267607152
PheGenIrs267607152
hapmaprs267607152
1000 genomesrs267607152
hgdprs267607152
ensemblrs267607152
gopubmedrs267607152
geneviewrs267607152
scholarrs267607152
googlers267607152
pharmgkbrs267607152
gwascentralrs267607152
openSNPrs267607152
23andMers267607152
23andMe allrs267607152
SNP Nexus

SNPshotrs267607152
SNPdbers267607152
MSV3drs267607152
GWAS Ctlgrs267607152
Max Magnitude0
ClinVar
Risk rs267607152(A;A)
Alt rs267607152(A;A)
Reference rs267607152(T;T)
Significance Pathogenic
Disease Exudative vitreoretinopathy 5
Variation info
Gene TSPAN12
CLNDBN Exudative vitreoretinopathy 5
Reversed 1
HGVS NC_000007.13:g.120455841A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000352.3,