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rs267607153

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607153(A;A)
Make rs267607153(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position120810512
GeneTSPAN12
is asnp
is mentioned by
dbSNPrs267607153
ebirs267607153
HLIrs267607153
Exacrs267607153
Varsomers267607153
Maprs267607153
PheGenIrs267607153
hapmaprs267607153
1000 genomesrs267607153
hgdprs267607153
ensemblrs267607153
gopubmedrs267607153
geneviewrs267607153
scholarrs267607153
googlers267607153
pharmgkbrs267607153
gwascentralrs267607153
openSNPrs267607153
23andMers267607153
23andMe allrs267607153
SNP Nexus

SNPshotrs267607153
SNPdbers267607153
MSV3drs267607153
GWAS Ctlgrs267607153
Max Magnitude0
ClinVar
Risk rs267607153(A;A)
Alt rs267607153(A;A)
Reference rs267607153(T;T)
Significance Pathogenic
Disease Exudative vitreoretinopathy 5
Variation info
Gene TSPAN12
CLNDBN Exudative vitreoretinopathy 5
Reversed 1
HGVS NC_000007.13:g.120450566A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000350.4,